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      <references>
        <reference>
          <otype>Reference</otype>
          <mtid>43948406</mtid>
          <link>/api/reference/43948406</link>
          <label>1. Mahesh, S., Tang, K.-C., and Raj, M. (2018). Amide Bond Activation of Biological Molecules. Molecules, 23., DOI: 10.3390/molecules23102615</label>
          <listPosition>1</listPosition>
          <doi>10.3390/molecules23102615</doi>
          <published>false</published>
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        <reference>
          <otype>Reference</otype>
          <mtid>43948407</mtid>
          <link>/api/reference/43948407</link>
          <label>2. Pattabiraman 2011: Rethinking amide bond synthesis., Nature, 480, p. 471, DOI: 10.1038/nature10702</label>
          <listPosition>2</listPosition>
          <doi>10.1038/nature10702</doi>
          <published>false</published>
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        <reference>
          <otype>Reference</otype>
          <mtid>43948408</mtid>
          <link>/api/reference/43948408</link>
          <label>3. Wieland, T., and Bodanszky, M. (2012). The World of Peptides: A Brief History of Peptide Chemistry, Springer.</label>
          <listPosition>3</listPosition>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948409</mtid>
          <link>/api/reference/43948409</link>
          <label>4. Ohashi 2020: Analgesic Effect of Acetaminophen: A Review of Known and Novel Mechanisms of Action., Front. Pharmacol., 11, p. 580289, DOI: 10.3389/fphar.2020.580289</label>
          <listPosition>4</listPosition>
          <doi>10.3389/fphar.2020.580289</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948410</mtid>
          <link>/api/reference/43948410</link>
          <label>5. Day 1991: The pharmacology of local anesthetics., Vet. Clin. N. Am. Large Anim. Pract., 7, p. 489</label>
          <listPosition>5</listPosition>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948411</mtid>
          <link>/api/reference/43948411</link>
          <label>6. Becker 2012: Local anesthetics: Review of pharmacological considerations., Anesth. Prog., 59, p. 90, DOI: 10.2344/0003-3006-59.2.90</label>
          <listPosition>6</listPosition>
          <doi>10.2344/0003-3006-59.2.90</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948412</mtid>
          <link>/api/reference/43948412</link>
          <label>7. Lima 2020: β-lactam antibiotics: An overview from a medicinal chemistry perspective., Eur. J. Med. Chem., 208, p. 112829, DOI: 10.1016/j.ejmech.2020.112829</label>
          <listPosition>7</listPosition>
          <doi>10.1016/j.ejmech.2020.112829</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948413</mtid>
          <link>/api/reference/43948413</link>
          <label>8. Turner 2022: The Chemical Relationship Among Beta-Lactam Antibiotics and Potential Impacts on Reactivity and Decomposition., Front. Microbiol., 13, p. 807955, DOI: 10.3389/fmicb.2022.807955</label>
          <listPosition>8</listPosition>
          <doi>10.3389/fmicb.2022.807955</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948414</mtid>
          <link>/api/reference/43948414</link>
          <label>9. King 2016: One ring to rule them all: Current trends in combating bacterial resistance to the β-lactams., Protein Sci., 25, p. 787, DOI: 10.1002/pro.2889</label>
          <listPosition>9</listPosition>
          <doi>10.1002/pro.2889</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948415</mtid>
          <link>/api/reference/43948415</link>
          <label>10. Saxena 2020: A journey of celecoxib from pain to cancer., Prostaglandins Other Lipid Mediat., 147, p. 106379, DOI: 10.1016/j.prostaglandins.2019.106379</label>
          <listPosition>10</listPosition>
          <doi>10.1016/j.prostaglandins.2019.106379</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948416</mtid>
          <link>/api/reference/43948416</link>
          <label>11. Bohn 2006: How specific are “target-specific” drugs? Celecoxib as a case in point., Mol. Interv., 6, p. 196, DOI: 10.1124/mi.6.4.5</label>
          <listPosition>11</listPosition>
          <doi>10.1124/mi.6.4.5</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948417</mtid>
          <link>/api/reference/43948417</link>
          <label>12. Bering 2022: Merging enzymes with chemocatalysis for amide bond synthesis., Nat. Commun., 13, p. 380, DOI: 10.1038/s41467-022-28005-4</label>
          <listPosition>12</listPosition>
          <doi>10.1038/s41467-022-28005-4</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948418</mtid>
          <link>/api/reference/43948418</link>
          <label>13. Allen 2011: Metal-catalysed approaches to amide bond formation., Chem. Soc. Rev., 40, p. 3405, DOI: 10.1039/c0cs00196a</label>
          <listPosition>13</listPosition>
          <doi>10.1039/c0cs00196a</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948419</mtid>
          <link>/api/reference/43948419</link>
          <label>14. Massolo 2020: Amide Bond Formation Strategies: Latest Advances on a Dateless Transformation., Eur. J. Org. Chem., 2020, p. 4641, DOI: 10.1002/ejoc.202000080</label>
          <listPosition>14</listPosition>
          <doi>10.1002/ejoc.202000080</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948420</mtid>
          <link>/api/reference/43948420</link>
          <label>15. Todorovic 2020: Recent developments in catalytic amide bond formation., Pept. Sci., 112, p. e24210, DOI: 10.1002/pep2.24210</label>
          <listPosition>15</listPosition>
          <doi>10.1002/pep2.24210</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948421</mtid>
          <link>/api/reference/43948421</link>
          <label>16. Albericio 2011: Peptide Coupling Reagents, More than a Letter Soup., Chem. Rev., 111, p. 6557, DOI: 10.1021/cr100048w</label>
          <listPosition>16</listPosition>
          <doi>10.1021/cr100048w</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948422</mtid>
          <link>/api/reference/43948422</link>
          <label>17. Valeur 2009: Amide bond formation: Beyond the myth of coupling reagents., Chem. Soc. Rev., 38, p. 606, DOI: 10.1039/B701677H</label>
          <listPosition>17</listPosition>
          <doi>10.1039/B701677H</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948423</mtid>
          <link>/api/reference/43948423</link>
          <label>18. Orsy 2020: Direct amide formation in a continuous-flow system mediated by carbon disulfide., Catal. Sci. Technol., 10, p. 7814, DOI: 10.1039/D0CY01603A</label>
          <listPosition>18</listPosition>
          <doi>10.1039/D0CY01603A</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948424</mtid>
          <link>/api/reference/43948424</link>
          <label>19. Lundberg 2014: Catalytic amide formation from non-activated carboxylic acids and amines., Chem. Soc. Rev., 43, p. 2714, DOI: 10.1039/C3CS60345H</label>
          <listPosition>19</listPosition>
          <doi>10.1039/C3CS60345H</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948425</mtid>
          <link>/api/reference/43948425</link>
          <label>20. Hazra 2022: Water: An Underestimated Solvent for Amide Bond-Forming Reactions., ACS Sustain. Chem. Eng., 10, p. 5299, DOI: 10.1021/acssuschemeng.2c00520</label>
          <listPosition>20</listPosition>
          <doi>10.1021/acssuschemeng.2c00520</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948426</mtid>
          <link>/api/reference/43948426</link>
          <label>21. Sabatini 2019: A green chemistry perspective on catalytic amide bond formation., Nat. Catal., 2, p. 10, DOI: 10.1038/s41929-018-0211-5</label>
          <listPosition>21</listPosition>
          <doi>10.1038/s41929-018-0211-5</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948427</mtid>
          <link>/api/reference/43948427</link>
          <label>22. Zhang 2021: A practical and sustainable protocol for direct amidation of unactivated esters under transition-metal-free and solvent-free conditions., Green Chem., 23, p. 3972, DOI: 10.1039/D1GC00720C</label>
          <listPosition>22</listPosition>
          <doi>10.1039/D1GC00720C</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948428</mtid>
          <link>/api/reference/43948428</link>
          <label>23. Dunetz 2016: Large-Scale Applications of Amide Coupling Reagents for the Synthesis of Pharmaceuticals., Org. Process Res. Dev., 20, p. 140, DOI: 10.1021/op500305s</label>
          <listPosition>23</listPosition>
          <doi>10.1021/op500305s</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948429</mtid>
          <link>/api/reference/43948429</link>
          <label>24. Magano 2022: Large-Scale Amidations in Process Chemistry: Practical Considerations for Reagent Selection and Reaction Execution Organic., Org. Process Res. Dev., 26, p. 1562, DOI: 10.1021/acs.oprd.2c00005</label>
          <listPosition>24</listPosition>
          <doi>10.1021/acs.oprd.2c00005</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948430</mtid>
          <link>/api/reference/43948430</link>
          <label>25. Ganesh 2021: Green Chemistry: A Framework for a Sustainable Future., Org. Process Res. Dev., 25, p. 1455, DOI: 10.1021/acs.oprd.1c00216</label>
          <listPosition>25</listPosition>
          <doi>10.1021/acs.oprd.1c00216</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948431</mtid>
          <link>/api/reference/43948431</link>
          <label>26. Anastas 2010: Green Chemistry: Principles and Practice., Chem. Soc. Rev., 39, p. 301, DOI: 10.1039/B918763B</label>
          <listPosition>26</listPosition>
          <doi>10.1039/B918763B</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948432</mtid>
          <link>/api/reference/43948432</link>
          <label>27. Meyer 2013: The use of enzymes in organic synthesis and the life sciences: Perspectives from the Swiss Industrial Biocatalysis Consortium (SIBC)., Catal. Sci. Technol., 3, p. 29, DOI: 10.1039/C2CY20350B</label>
          <listPosition>27</listPosition>
          <doi>10.1039/C2CY20350B</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948433</mtid>
          <link>/api/reference/43948433</link>
          <label>28. Silverman, R.B. (2002). Organic Chemistry of Enzyme-Catalyzed Reactions, Academic Press. [2nd ed.].</label>
          <listPosition>28</listPosition>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948434</mtid>
          <link>/api/reference/43948434</link>
          <label>29. Strohmeier 2011: Application of Designed Enzymes in Organic Synthesis., Chem. Rev., 111, p. 4141, DOI: 10.1021/cr100386u</label>
          <listPosition>29</listPosition>
          <doi>10.1021/cr100386u</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948435</mtid>
          <link>/api/reference/43948435</link>
          <label>30. Winkler 2021: Power of Biocatalysis for Organic Synthesis., ACS Cent. Sci., 7, p. 55, DOI: 10.1021/acscentsci.0c01496</label>
          <listPosition>30</listPosition>
          <doi>10.1021/acscentsci.0c01496</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948436</mtid>
          <link>/api/reference/43948436</link>
          <label>31. 2004: Advanced procedure for the enzymatic ring opening of unsaturated alicyclic β-lactams., Tetrahedron Asymmetry, 15, p. 2875, DOI: 10.1016/j.tetasy.2004.05.029</label>
          <listPosition>31</listPosition>
          <doi>10.1016/j.tetasy.2004.05.029</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948437</mtid>
          <link>/api/reference/43948437</link>
          <label>32. Shoda 2016: Enzymes as Green Catalysts for Precision Macromolecular Synthesis., Chem. Rev., 116, p. 2307, DOI: 10.1021/acs.chemrev.5b00472</label>
          <listPosition>32</listPosition>
          <doi>10.1021/acs.chemrev.5b00472</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948438</mtid>
          <link>/api/reference/43948438</link>
          <label>33. Sheldon 2016: Engineering a more sustainable world through catalysis and green chemistry., J. R. Soc. Interface, 13, p. 20160087, DOI: 10.1098/rsif.2016.0087</label>
          <listPosition>33</listPosition>
          <doi>10.1098/rsif.2016.0087</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948439</mtid>
          <link>/api/reference/43948439</link>
          <label>34. Augustin 2019: Enzyme morphinan N-demethylase for more sustainable opiate processing., Nat. Sustain., 2, p. 465, DOI: 10.1038/s41893-019-0302-6</label>
          <listPosition>34</listPosition>
          <doi>10.1038/s41893-019-0302-6</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948440</mtid>
          <link>/api/reference/43948440</link>
          <label>35. Sheldon 2022: Green Chemistry, Biocatalysis, and the Chemical Industry of the Future., ChemSusChem, 15, p. e202102628, DOI: 10.1002/cssc.202102628</label>
          <listPosition>35</listPosition>
          <doi>10.1002/cssc.202102628</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948441</mtid>
          <link>/api/reference/43948441</link>
          <label>36. Stergiou 2013: Advances in lipase-catalyzed esterification reactions., Biotechnol. Adv., 31, p. 1846, DOI: 10.1016/j.biotechadv.2013.08.006</label>
          <listPosition>36</listPosition>
          <doi>10.1016/j.biotechadv.2013.08.006</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948442</mtid>
          <link>/api/reference/43948442</link>
          <label>37. Gamayurova 2021: Lipases in Esterification Reactions: A Review., Catal. Ind., 13, p. 58, DOI: 10.1134/S2070050421010025</label>
          <listPosition>37</listPosition>
          <doi>10.1134/S2070050421010025</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948443</mtid>
          <link>/api/reference/43948443</link>
          <label>38. Singhania 2022: Lipase-catalyzed esterification in water enabled by nanomicelles. Applications to 1-pot multi-step sequences., Chem. Sci., 13, p. 1440, DOI: 10.1039/D1SC05660C</label>
          <listPosition>38</listPosition>
          <doi>10.1039/D1SC05660C</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948444</mtid>
          <link>/api/reference/43948444</link>
          <label>39. Kumar 2016: Lipase catalysis in organic solvents: Advantages and applications., Biol. Proced. Online, 18, p. 2, DOI: 10.1186/s12575-016-0033-2</label>
          <listPosition>39</listPosition>
          <doi>10.1186/s12575-016-0033-2</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948445</mtid>
          <link>/api/reference/43948445</link>
          <label>40. Ingenbosch 2022: Effect of Organic Solvents on the Structure and Activity of a Minimal Lipase., J. Org. Chem., 87, p. 1669, DOI: 10.1021/acs.joc.1c01136</label>
          <listPosition>40</listPosition>
          <doi>10.1021/acs.joc.1c01136</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948446</mtid>
          <link>/api/reference/43948446</link>
          <label>41. Ortiz 2019: Novozym 435: The “perfect” lipase immobilized biocatalyst?., Catal. Sci. Technol., 9, p. 2380, DOI: 10.1039/C9CY00415G</label>
          <listPosition>41</listPosition>
          <doi>10.1039/C9CY00415G</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948447</mtid>
          <link>/api/reference/43948447</link>
          <label>42. Mangiagalli 2020: Diverse effects of aqueous polar co-solvents on Candida antarctica lipase B., Int. J. Biol. Macromol., 150, p. 930, DOI: 10.1016/j.ijbiomac.2020.02.145</label>
          <listPosition>42</listPosition>
          <doi>10.1016/j.ijbiomac.2020.02.145</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948448</mtid>
          <link>/api/reference/43948448</link>
          <label>43. Zieniuk 2020: Screening of solvents for favoring hydrolytic activity of Candida antarctica Lipase B., Bioprocess Biosyst. Eng., 43, p. 605, DOI: 10.1007/s00449-019-02252-0</label>
          <listPosition>43</listPosition>
          <doi>10.1007/s00449-019-02252-0</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948449</mtid>
          <link>/api/reference/43948449</link>
          <label>44. 2022: Enzymatic Strategies for the Preparation of Pharmaceutically Important Amino Acids through Hydrolysis of Amino Carboxylic Esters and Lactams., Curr. Med. Chem., 29, p. 6218, DOI: 10.2174/0929867329666220718123153</label>
          <listPosition>44</listPosition>
          <doi>10.2174/0929867329666220718123153</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948450</mtid>
          <link>/api/reference/43948450</link>
          <label>45. Megyesi 2018: Substrate engineering: Effects of different N-protecting groups in the CAL-B-catalysed asymmetric O-acylation of 1-hydroxymethyl-tetrahydro-β-carbolines., Tetrahedron, 74, p. 2634, DOI: 10.1016/j.tet.2018.04.012</label>
          <listPosition>45</listPosition>
          <doi>10.1016/j.tet.2018.04.012</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948451</mtid>
          <link>/api/reference/43948451</link>
          <label>46. Shahmohammadi, S., Faragó, T., Palkó, M., and Forró, E. (2022). Green Strategies for the Preparation of Enantiomeric 5–8-Membered Carbocyclic β-Amino Acid Derivatives through CALB-Catalyzed Hydrolysis. Molecules, 27., DOI: 10.3390/molecules27082600</label>
          <listPosition>46</listPosition>
          <doi>10.3390/molecules27082600</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948452</mtid>
          <link>/api/reference/43948452</link>
          <label>47. Sun 2020: Optimization of the Lipase-Catalyzed Selective Amidation of Phenylglycinol., Front. Bioeng. Biotechnol., 7, p. 486, DOI: 10.3389/fbioe.2019.00486</label>
          <listPosition>47</listPosition>
          <doi>10.3389/fbioe.2019.00486</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948453</mtid>
          <link>/api/reference/43948453</link>
          <label>48. Pitzer 2022: Racemization-free and scalable amidation of l-proline in organic media using ammonia and a biocatalyst only., Green Chem., 24, p. 5171, DOI: 10.1039/D2GC00783E</label>
          <listPosition>48</listPosition>
          <doi>10.1039/D2GC00783E</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948454</mtid>
          <link>/api/reference/43948454</link>
          <label>49. Hassan 2013: Three-component chemoenzymatic synthesis of amide ligated 1,2,3-triazoles., Tetrahedron Lett., 54, p. 4641, DOI: 10.1016/j.tetlet.2013.06.051</label>
          <listPosition>49</listPosition>
          <doi>10.1016/j.tetlet.2013.06.051</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948455</mtid>
          <link>/api/reference/43948455</link>
          <label>50. Irimescu 2004: Lipase-catalyzed enantioselective reaction of amines with carboxylic acids under reduced pressure in non-solvent system and in ionic liquids., Tetrahedron Lett., 45, p. 523, DOI: 10.1016/j.tetlet.2003.10.210</label>
          <listPosition>50</listPosition>
          <doi>10.1016/j.tetlet.2003.10.210</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948456</mtid>
          <link>/api/reference/43948456</link>
          <label>51. Prasad 2005: Solvent-free biocatalytic amidation of carboxylic acids., Tetrahedron Lett., 46, p. 4511, DOI: 10.1016/j.tetlet.2005.04.121</label>
          <listPosition>51</listPosition>
          <doi>10.1016/j.tetlet.2005.04.121</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948457</mtid>
          <link>/api/reference/43948457</link>
          <label>52. Gotor 1999: Non-conventional hydrolase chemistry: Amide and carbamate bond formation catalyzed by lipases., Bioorg. Med. Chem., 7, p. 2189, DOI: 10.1016/S0968-0896(99)00150-9</label>
          <listPosition>52</listPosition>
          <doi>10.1016/S0968-0896(99)00150-9</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948458</mtid>
          <link>/api/reference/43948458</link>
          <label>53. Manova 2018: Lipase-catalyzed amidation of carboxylic acid and amines., Tetrahedron Lett., 59, p. 2086, DOI: 10.1016/j.tetlet.2018.04.049</label>
          <listPosition>53</listPosition>
          <doi>10.1016/j.tetlet.2018.04.049</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948459</mtid>
          <link>/api/reference/43948459</link>
          <label>54. Dorr 2018: Enzymatic amidation for industrial applications., Curr. Opin. Chem. Biol., 43, p. 127, DOI: 10.1016/j.cbpa.2018.01.008</label>
          <listPosition>54</listPosition>
          <doi>10.1016/j.cbpa.2018.01.008</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948460</mtid>
          <link>/api/reference/43948460</link>
          <label>55. Lima 2019: Versatility of Candida antarctica lipase in the amide bond formation applied in organic synthesis and biotechnological processes., Mol. Catal., 466, p. 75, DOI: 10.1016/j.mcat.2019.01.007</label>
          <listPosition>55</listPosition>
          <doi>10.1016/j.mcat.2019.01.007</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948461</mtid>
          <link>/api/reference/43948461</link>
          <label>56. Lo, Y.C., Lin, C.L., Fang, W.Y., Lőrinczi, B., Szatmári, I., Chang, W.H., Fülöp, F., and Wu, S.N. (2021). Effective Activation by Kynurenic Acid and Its Aminoalkylated Derivatives on M-Type K+ Current. Int. J. Mol. Sci., 22., DOI: 10.3390/ijms22031300</label>
          <listPosition>56</listPosition>
          <doi>10.3390/ijms22031300</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948462</mtid>
          <link>/api/reference/43948462</link>
          <label>57. Hollmann 2018: Biocatalytic synthesis of lactones and lactams., Chem.-Asian J., 13, p. 3601, DOI: 10.1002/asia.201801180</label>
          <listPosition>57</listPosition>
          <doi>10.1002/asia.201801180</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948463</mtid>
          <link>/api/reference/43948463</link>
          <label>58. Kunishima 2004: Substrate-Specific Amidation of Carboxylic Acids in a Liquid-Liquid Two-Phase System Using Cyclodextrins as Inverse Phase-Transfer Catalysts., Eur. J. Org. Chem., 2004, p. 4535, DOI: 10.1002/ejoc.200400470</label>
          <listPosition>58</listPosition>
          <doi>10.1002/ejoc.200400470</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948464</mtid>
          <link>/api/reference/43948464</link>
          <label>59. Kim 2016: A Versatile Cobalt Catalyst for Secondary and Tertiary Amide Synthesis from Various Carboxylic Acid Derivatives., Asian J. Org. Chem., 5, p. 222, DOI: 10.1002/ajoc.201500444</label>
          <listPosition>59</listPosition>
          <doi>10.1002/ajoc.201500444</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948465</mtid>
          <link>/api/reference/43948465</link>
          <label>60. 2015: Direct amidation of carboxylic acids with amines under microwave irradiation using silica gel as a solid support., Green Chem., 17, p. 3157, DOI: 10.1039/C5GC00189G</label>
          <listPosition>60</listPosition>
          <doi>10.1039/C5GC00189G</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948466</mtid>
          <link>/api/reference/43948466</link>
          <label>61. Bonnamour 2015: Comprehensive Study of the Organic Solvent-Free CDI-Mediated Acylation of Various Nucleophiles by Mechanochemistry., Chem. Eur. J., 21, p. 12787, DOI: 10.1002/chem.201501325</label>
          <listPosition>61</listPosition>
          <doi>10.1002/chem.201501325</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948467</mtid>
          <link>/api/reference/43948467</link>
          <label>62. Roe 1951: Fatty Acid Amides. III.2a N-Alkenyl and N,N-Dialkenyl Amides2b., J. Am. Chem. Soc., 73, p. 3642, DOI: 10.1021/ja01152a024</label>
          <listPosition>62</listPosition>
          <doi>10.1021/ja01152a024</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948468</mtid>
          <link>/api/reference/43948468</link>
          <label>63. Willand 2010: Exploring Drug Target Flexibility Using in Situ Click Chemistry: Application to a Mycobacterial Transcriptional Regulator., ACS Chem. Biol., 5, p. 1007, DOI: 10.1021/cb100177g</label>
          <listPosition>63</listPosition>
          <doi>10.1021/cb100177g</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948469</mtid>
          <link>/api/reference/43948469</link>
          <label>64. Tian 2012: Recyclable Hypervalent Iodine(III) Reagent Iodosodilactone as an Efficient Coupling Reagent for Direct Esterification, Amidation, and Peptide Coupling., Org. Lett., 14, p. 3020, DOI: 10.1021/ol301085v</label>
          <listPosition>64</listPosition>
          <doi>10.1021/ol301085v</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948470</mtid>
          <link>/api/reference/43948470</link>
          <label>65. Ouerghui 2016: Chemical modifications of poly(vinyl chloride) to poly(vinyl azide) and “clicked” triazole bearing groups for application in metal cation extraction., Adv. Mater. Res., 100, p. 191</label>
          <listPosition>65</listPosition>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948471</mtid>
          <link>/api/reference/43948471</link>
          <label>66. Wei 2012: Direct use of dioxygen as an oxygen source: Catalytic oxidative synthesis of amides., Chem. Commun., 48, p. 305, DOI: 10.1039/C1CC14640H</label>
          <listPosition>66</listPosition>
          <doi>10.1039/C1CC14640H</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
        <reference>
          <otype>Reference</otype>
          <mtid>43948472</mtid>
          <link>/api/reference/43948472</link>
          <label>67. Cromwell 1956: Studies with the Amine Adducts of β-Benzoylacrylic Acid and its Methyl Ester., J. Am. Chem. Soc., 78, p. 4412, DOI: 10.1021/ja01598a058</label>
          <listPosition>67</listPosition>
          <doi>10.1021/ja01598a058</doi>
          <published>false</published>
          <snippet>true</snippet>
        </reference>
      </references>
      <link>/api/publication/34082152</link>
      <label>Orsy György et al. A Sustainable Green Enzymatic Method for Amide Bond Formation. 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&lt;span class=&quot;authorAux-mtmt&quot;&gt; áramlásos kémia&lt;/span&gt;) &lt;/a&gt; &lt;/span&gt; &lt;span class=&quot;author-affil&quot;&gt;&lt;span title=&quot;Szegedi Tudományegyetem&quot;&gt;SZTE&lt;/span&gt;/&lt;span title=&quot;Gyógyszerésztudományi Kar&quot;&gt;GYTK&lt;/span&gt;/Gyógyszerkémiai Intézet&lt;/span&gt; ;&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;span class=&quot;author-name&quot; mtid=&quot;10082825&quot;&gt;&lt;a href=&quot;/gui2/?type=authors&amp;mode=browse&amp;sel=10082825&quot; target=&quot;_blank&quot;&gt;Shahmohammadi Sayeh (&lt;span class=&quot;authorship-author-name&quot;&gt;Shahmohammadi Sayeh&lt;/span&gt; &lt;span class=&quot;authorAux-mtmt&quot;&gt; Pharmaceutical Chemistry&lt;/span&gt;) &lt;/a&gt; &lt;/span&gt; &lt;span class=&quot;author-affil&quot;&gt;&lt;span title=&quot;Szegedi Tudományegyetem&quot;&gt;SZTE&lt;/span&gt;/&lt;span title=&quot;Gyógyszerésztudományi Kar&quot;&gt;GYTK&lt;/span&gt;/Gyógyszerkémiai Intézet; &lt;span title=&quot;Szegedi Tudományegyetem&quot;&gt;SZTE&lt;/span&gt;/&lt;span title=&quot;Gyógyszerésztudományi Kar&quot;&gt;GYTK&lt;/span&gt;/&lt;span title=&quot;Gyógyszerkémiai Intézet&quot;&gt;GYKI&lt;/span&gt;/ELKH-SZTE Sztereokémiai Kutatócsoport&lt;/span&gt; ;&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;span class=&quot;author-name&quot; mtid=&quot;10002835&quot;&gt;&lt;a href=&quot;/gui2/?type=authors&amp;mode=browse&amp;sel=10002835&quot; target=&quot;_blank&quot;&gt;Forró Enikő ✉ (&lt;span class=&quot;authorship-author-name&quot;&gt;Forró Enikő&lt;/span&gt; &lt;span class=&quot;authorAux-mtmt&quot;&gt; Szerves kémia&lt;/span&gt;) &lt;/a&gt; &lt;/span&gt; &lt;span class=&quot;author-affil&quot;&gt;&lt;span title=&quot;Szegedi Tudományegyetem&quot;&gt;SZTE&lt;/span&gt;/&lt;span title=&quot;Gyógyszerésztudományi Kar&quot;&gt;GYTK&lt;/span&gt;/Gyógyszerkémiai Intézet&lt;/span&gt; &lt;/div&gt; &lt;/div&gt; &lt;div class=&quot;title&quot;&gt;&lt;a href=&quot;/gui2/?mode=browse&amp;params=publication;34082152&quot; target=&quot;_blank&quot;&gt;A Sustainable Green Enzymatic Method for Amide Bond Formation&lt;/a&gt;&lt;/div&gt; &lt;div&gt; &lt;span class=&quot;journal-title&quot;&gt;MOLECULES&lt;/span&gt; &lt;span class=&quot;journal-issn&quot;&gt;(&lt;a target=&quot;_blank&quot; href=&quot;https://portal.issn.org/resource/ISSN/1431-5157&quot;&gt;1431-5157&lt;/a&gt; &lt;a target=&quot;_blank&quot; href=&quot;https://portal.issn.org/resource/ISSN/1420-3049&quot;&gt;1420-3049&lt;/a&gt;)&lt;/span&gt;: &lt;span class=&quot;journal-volume&quot;&gt;28&lt;/span&gt; &lt;span class=&quot;journal-issue&quot;&gt;15&lt;/span&gt; &lt;span class=&quot;page&quot;&gt; Paper 5706. 11 p. &lt;/span&gt; &lt;span class=&quot;year&quot;&gt;(2023)&lt;/span&gt; &lt;/div&gt; &lt;div class=&quot;pub-footer&quot;&gt;  &lt;span class=&quot;language&quot; xmlns=&quot;http://www.w3.org/1999/html&quot;&gt;Nyelv: Angol | &lt;/span&gt; &lt;span class=&quot;identifiers&quot;&gt; &lt;span class=&quot;id identifier oa_none&quot; title=&quot;none&quot;&gt; &lt;a style=&quot;color:blue&quot; title=&quot;10.3390/molecules28155706&quot; target=&quot;_blank&quot; href=&quot;https://doi.org/10.3390/molecules28155706&quot;&gt; DOI &lt;/a&gt; &lt;/span&gt; &lt;span class=&quot;id identifier oa_none&quot; title=&quot;none&quot;&gt; &lt;a style=&quot;color:blue&quot; title=&quot;001046260900001&quot; target=&quot;_blank&quot; href=&quot;https://www.webofscience.com/wos/woscc/full-record/001046260900001&quot;&gt; WoS &lt;/a&gt; &lt;/span&gt; &lt;span class=&quot;id identifier oa_none&quot; title=&quot;none&quot;&gt; &lt;a style=&quot;color:blue&quot; title=&quot;85167744946&quot; target=&quot;_blank&quot; href=&quot;http://www.scopus.com/record/display.url?origin=inward&amp;eid=2-s2.0-85167744946&quot;&gt; Scopus &lt;/a&gt; &lt;/span&gt; &lt;span class=&quot;id identifier oa_none&quot; title=&quot;none&quot;&gt; &lt;a style=&quot;color:blue&quot; title=&quot;37570676&quot; target=&quot;_blank&quot; href=&quot;http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&amp;db=PubMed&amp;list_uids=37570676&amp;dopt=Abstract&quot;&gt; PubMed &lt;/a&gt; &lt;/span&gt; &lt;span class=&quot;id identifier oa_none&quot; title=&quot;none&quot;&gt; &lt;a style=&quot;color:black&quot; title=&quot;https://www.mdpi.com/1420-3049/28/15/5706&quot; target=&quot;_blank&quot; href=&quot;https://www.mdpi.com/1420-3049/28/15/5706&quot;&gt; Egyéb URL &lt;/a&gt; &lt;/span&gt; &lt;span class=&quot;id identifier oa_GREEN&quot; title=&quot; Green &quot;&gt; &lt;a style=&quot;color:blue&quot; title=&quot;28021&quot; target=&quot;_blank&quot; href=&quot;http://publicatio.bibl.u-szeged.hu/28021&quot;&gt; SZTE Publicatio &lt;/a&gt; &lt;/span&gt; &lt;/span&gt; &lt;OnlyViewableByAuthor&gt;&lt;div class=&quot;ratings&quot;&gt; &lt;div class=&quot;journal-subject&quot;&gt;Folyóirat szakterülete: Scopus - Analytical Chemistry&amp;nbsp;&amp;nbsp;&amp;nbsp;SJR indikátor:&amp;nbsp;Q1&lt;/div&gt; &lt;div class=&quot;journal-subject&quot;&gt;Folyóirat szakterülete: Scopus - Chemistry (miscellaneous)&amp;nbsp;&amp;nbsp;&amp;nbsp;SJR indikátor:&amp;nbsp;Q1&lt;/div&gt; &lt;div class=&quot;journal-subject&quot;&gt;Folyóirat szakterülete: Scopus - Pharmaceutical Science&amp;nbsp;&amp;nbsp;&amp;nbsp;SJR indikátor:&amp;nbsp;Q1&lt;/div&gt; &lt;div class=&quot;journal-subject&quot;&gt;Folyóirat szakterülete: Scopus - Drug Discovery&amp;nbsp;&amp;nbsp;&amp;nbsp;SJR indikátor:&amp;nbsp;Q2&lt;/div&gt; &lt;div class=&quot;journal-subject&quot;&gt;Folyóirat szakterülete: Scopus - Medicine (miscellaneous)&amp;nbsp;&amp;nbsp;&amp;nbsp;SJR indikátor:&amp;nbsp;Q2&lt;/div&gt; &lt;div class=&quot;journal-subject&quot;&gt;Folyóirat szakterülete: Scopus - Organic Chemistry&amp;nbsp;&amp;nbsp;&amp;nbsp;SJR indikátor:&amp;nbsp;Q2&lt;/div&gt; &lt;div class=&quot;journal-subject&quot;&gt;Folyóirat szakterülete: Scopus - Physical and Theoretical Chemistry&amp;nbsp;&amp;nbsp;&amp;nbsp;SJR indikátor:&amp;nbsp;Q2&lt;/div&gt; &lt;div class=&quot;journal-subject&quot;&gt;Folyóirat szakterülete: Scopus - Molecular Medicine&amp;nbsp;&amp;nbsp;&amp;nbsp;SJR indikátor:&amp;nbsp;Q3&lt;/div&gt; &lt;/div&gt;&lt;/OnlyViewableByAuthor&gt; &lt;div class=&quot;publication-citation&quot; style=&quot;margin-left: 0.5cm;&quot;&gt; &lt;span title=&quot;Nyilvános idézőközlemények összesen, említések nélkül&quot; class=&quot;citingPub-count&quot;&gt;Nyilvános idéző összesen: 6&lt;/span&gt; | Független: 6 | Függő: 0 | Nem jelölt: 0 | WoS jelölt: 6 | Scopus jelölt:&amp;nbsp;6 | WoS/Scopus jelölt:&amp;nbsp;6 | DOI jelölt:&amp;nbsp;6 &lt;/div&gt;   &lt;div class=&quot;publication-citation&quot;&gt; &lt;a target=&quot;_blank&quot; href=&quot;/api/publication?cond=citations.related;eq;34082152&amp;sort=publishedYear,desc&amp;sort=title&quot;&gt; Idézett közlemények száma: 6 &lt;/a&gt; &lt;/div&gt; &lt;div class=&quot;mtid&quot;&gt;&lt;span class=&quot;long-pub-mtid&quot;&gt;Közlemény: 34082152&lt;/span&gt; | &lt;span class=&quot;status-data status-VALIDATED&quot;&gt; Egyeztetett &lt;/span&gt; Forrás Idéző | &lt;span class=&quot;type-subtype&quot;&gt;Folyóiratcikk ( Szakcikk ) &lt;/span&gt; | &lt;span class=&quot;pub-category&quot;&gt;Tudományos&lt;/span&gt; | &lt;span class=&quot;publication-sourceOfData&quot;&gt;kézi felvitel&lt;/span&gt; &lt;/div&gt; &lt;div class=&quot;funder&quot;&gt; (K 138871) Támogató: NKFI, (TKP2021-EGA-32) Támogató: NKFIH &lt;/div&gt; &lt;div class=&quot;lastModified&quot;&gt;Utolsó módosítás: 2026.03.06. 20:50 Pécsi Éva (MTMT Közp 2,3, admin) &lt;/div&gt; &lt;/div&gt;&lt;/div&gt;</template2>
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