@article{MTMT:32782961,
	title = {Valerii V. Lunin (ed): The Chemistry Department of Moscow State University, Its Three Quarters of a Century (in Russian, Khimicheskii Fakul’tet MGU: Put’ v tri chetverti veka)},
	url = {https://m2.mtmt.hu/api/publication/32782961},
	author = {Hargittai, István},
	doi = {10.1007/s11224-006-9124-z},
	journal-iso = {STRUCT CHEM},
	journal = {STRUCTURAL CHEMISTRY},
	volume = {17},
	unique-id = {32782961},
	issn = {1040-0400},
	year = {2006},
	eissn = {1572-9001},
	pages = {669-669}
}

@article{MTMT:32782958,
	title = {William Taussig Scott and Martin X. Moleski: Michael Polanyi, Scientist and Philosopher. Oxford University Press, 2005},
	url = {https://m2.mtmt.hu/api/publication/32782958},
	author = {Hargittai, István},
	doi = {10.1007/s11224-006-9056-7},
	journal-iso = {STRUCT CHEM},
	journal = {STRUCTURAL CHEMISTRY},
	volume = {17},
	unique-id = {32782958},
	issn = {1040-0400},
	year = {2006},
	eissn = {1572-9001},
	pages = {551-552}
}

@article{MTMT:32782956,
	title = {Andrew Brown: J. D. Bernal, The Sage of Science, Oxford University Press, 2005},
	url = {https://m2.mtmt.hu/api/publication/32782956},
	author = {Hargittai, István},
	doi = {10.1007/s11224-006-9055-8},
	journal-iso = {STRUCT CHEM},
	journal = {STRUCTURAL CHEMISTRY},
	volume = {17},
	unique-id = {32782956},
	issn = {1040-0400},
	year = {2006},
	eissn = {1572-9001},
	pages = {451-452}
}

@article{MTMT:32782950,
	title = {Köhler’s Invention Klaus Eichmann (Max-Planck-Institut für Immunbiologie, Freiburg, Germany), Birkhäuser Verlag, Basel. 2005. 223 pp. USD 65.95; EUR 51.36. ISBN 3-7643-7173-0},
	url = {https://m2.mtmt.hu/api/publication/32782950},
	author = {Hargittai, István},
	doi = {10.1007/s11224-006-9042-0},
	journal-iso = {STRUCT CHEM},
	journal = {STRUCTURAL CHEMISTRY},
	volume = {17},
	unique-id = {32782950},
	issn = {1040-0400},
	year = {2006},
	eissn = {1572-9001},
	pages = {161-162}
}

@article{MTMT:32782948,
	title = {Nancy Thorndike Greenspan: The End of the Certain World. The Life and Science of Max Born: The Nobel Physicist Who Ignited the Quantum Revolution},
	url = {https://m2.mtmt.hu/api/publication/32782948},
	author = {Hargittai, István},
	doi = {10.1007/s11224-006-9039-8},
	journal-iso = {STRUCT CHEM},
	journal = {STRUCTURAL CHEMISTRY},
	volume = {17},
	unique-id = {32782948},
	issn = {1040-0400},
	year = {2006},
	eissn = {1572-9001},
	pages = {157-159}
}

@article{MTMT:2826571,
	title = {Qualification of assessors in food profile analysis and other new developments of ProfiSens},
	url = {https://m2.mtmt.hu/api/publication/2826571},
	author = {Heszberger, J and Papp, E and Kollárné Hunek, Klára and Kókai, Zoltán},
	journal-iso = {PERIOD POLYTECH CHEM ENG},
	journal = {PERIODICA POLYTECHNICA-CHEMICAL ENGINEERING},
	volume = {50},
	unique-id = {2826571},
	issn = {0324-5853},
	year = {2006},
	eissn = {1587-3765},
	pages = {95-107}
}

@article{MTMT:2638275,
	title = {NMR spectroscopic structure elucidation of the products of the reaction of 3-(3-aryl-3-oxopropenyl)-chromen-4-ones with 1,2-phenylenediamine},
	url = {https://m2.mtmt.hu/api/publication/2638275},
	author = {Tóth, Gábor and Simon, András and Gondos, T and Levai, A and Jekő, József and Andrasi, F},
	doi = {10.1002/mrc.1863},
	journal-iso = {MAGN RESON CHEM},
	journal = {MAGNETIC RESONANCE IN CHEMISTRY},
	volume = {44},
	unique-id = {2638275},
	issn = {0749-1581},
	abstract = {The reaction of 3-(3-aryl-3-oxopropenyl)chromen-4-ones with
		1,2-phenylenediamine resulted in the unexpected formation of
		10a-aryl-1,2,10,10a-tetrahydrobenzo-[4,5]-imidazo[1,2-alpyridin-3-yl(2-h
		ydroxyphenyl)-1-methanones. Their structure elucidation and complete
		111 and 13 C assignments have been performed by a combination of
		various one- and two-dimensional NMR experiments. Copyright (c) 2006
		John Wiley & Sons, Ltd.},
	year = {2006},
	eissn = {1097-458X},
	pages = {856-860}
}

@article{MTMT:2638274,
	title = {Glycosides from Bougainvillea glabra},
	url = {https://m2.mtmt.hu/api/publication/2638274},
	author = {Simon, András and Tóth, Gábor and Duddeck, H and Soliman, HSM and Mahmoud, II and Samir, H},
	doi = {10.1080/14786410500162351},
	journal-iso = {NAT PROD RES},
	journal = {NATURAL PRODUCT RESEARCH},
	volume = {20},
	unique-id = {2638274},
	issn = {1478-6419},
	abstract = {Three glycosides were isolated from Bougainvillea glabra and their
		structures were determined by extensive use of 1D and 2D NMR
		spectroscopy (H-1 and C-13). Compound 1 was identical to momordin IIc
		(quinoside D) [beta-D-glucopyranosyl 3-O-[beta-D-xylopyranosyl-(1 ->
		3)-O-(beta-D-glucopyranosyluronic acid)] oleanolate], compound 2 was
		quercetin 3-O-alpha-L-(rhamnopyranosyl)(1 ->
		6)-[alpha-L-rhamnopy-ranosyl(1 -> 2)]-beta-D-galactopyranoside and
		compound 3 was its derivative quercetin
		3-O-alpha-L-(4-caffeoylrhamnopyranosyl)(1 ->
		6)-[alpha-L-rhamnopyranosyl (1 -> 2)]-beta-D-galactopyranoside, a new
		natural product.},
	year = {2006},
	eissn = {1478-6427},
	pages = {63-67}
}

@article{MTMT:2638272,
	title = {Chiral atropisomeric 2-iodo-4,4',6,6'-tetramethyl-2'-(diphenylphosphoryl)-1,1'-biphenyl-enant iodifferentiation by Rh-2[MTPA](4)-adduct formation and conformational analysis},
	url = {https://m2.mtmt.hu/api/publication/2638272},
	author = {Moeller, S and Albert, D and Duddeck, H and Simon, András and Tóth, Gábor and Demchuk, OM and Pietrusiewicz, KM},
	doi = {10.1080/104265091000534},
	journal-iso = {PHOSPHOR SULFUR SIL REL ELEM},
	journal = {PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS},
	volume = {181},
	unique-id = {2638272},
	issn = {1042-6507},
	abstract = {Enantiodifferentiation of the chiral
		2-iodo-4,4',6,6'-tetramethyl-2'-(diphenylphosphoryl)1,1'-biphenyl (2)
		can be accomplished easily by adding one mole equivalent of the
		enantiopure dirhodium complex Rh-(II) (2)[(R)-(+)-MTPA](4) (Rh*). The
		internal competition of the two bindings sites in 2, the Ph-2 P=O
		group, and the iodine atom was identified by variable-temperature P-31
		NMR. Energy optimization (PM3) and ROESY spectroscopy of 2 in the
		absence and presence of Rh* reveal that 2 prefers a conformation in the
		adducts, which is the least stable one in the free molecule, i.e.,
		adduct formation is accompanied by a rotation of the Ph-2 P=O group
		about the C-2'-P bond.},
	year = {2006},
	eissn = {1563-5325},
	pages = {351-361}
}

@article{MTMT:1811472,
	title = {Reductive formation of 1,5-benzothiazeoines},
	url = {https://m2.mtmt.hu/api/publication/1811472},
	author = {A, Lévai and Tóth, Gábor and T, Gondos and Jekő, József and D I, Brahmhatt},
	doi = {10.3987/COM-06-10702},
	journal-iso = {HETEROCYCLES},
	journal = {HETEROCYCLES},
	volume = {68},
	unique-id = {1811472},
	issn = {0385-5414},
	year = {2006},
	eissn = {1881-0942},
	pages = {1319-1324}
}