@article{MTMT:36203475,
	title = {Lipase-catalyzed Strategies for the Preparation of Key Intermediates for the Synthesis of the Taxol Side Chain},
	url = {https://m2.mtmt.hu/api/publication/36203475},
	author = {Shahmohammadi, Sayeh and Orsy, György and Forró, Enikő},
	doi = {10.2174/0118756298317278240913071521},
	journal-iso = {MINI-REV ORG CHEM},
	journal = {MINI-REVIEWS IN ORGANIC CHEMISTRY},
	volume = {23},
	unique-id = {36203475},
	issn = {1570-193X},
	year = {2026},
	eissn = {1875-6298},
	pages = {1-9},
	orcid-numbers = {Shahmohammadi, Sayeh/0000-0001-7681-5458; Forró, Enikő/0000-0001-6796-3889}
}

@article{MTMT:34082152,
	title = {A Sustainable Green Enzymatic Method for Amide Bond Formation},
	url = {https://m2.mtmt.hu/api/publication/34082152},
	author = {Orsy, György and Shahmohammadi, Sayeh and Forró, Enikő},
	doi = {10.3390/molecules28155706},
	journal-iso = {MOLECULES},
	journal = {MOLECULES},
	volume = {28},
	unique-id = {34082152},
	issn = {1431-5157},
	abstract = {A sustainable enzymatic strategy for the preparation of amides by using Candida antarctica lipase B as the biocatalyst and cyclopentyl methyl ether as a green and safe solvent was devised. The method is simple and efficient and it produces amides with excellent conversions and yields without the need for intensive purification steps. The scope of the reaction was extended to the preparation of 28 diverse amides using four different free carboxylic acids and seven primary and secondary amines, including cyclic amines. This enzymatic methodology has the potential to become a green and industrially reliable process for direct amide synthesis.},
	year = {2023},
	eissn = {1420-3049},
	orcid-numbers = {Shahmohammadi, Sayeh/0000-0001-7681-5458; Forró, Enikő/0000-0001-6796-3889}
}

@article{MTMT:34320436,
	title = {Ancient complexes of iron and sulfur modulate oncogenes and oncometabolism},
	url = {https://m2.mtmt.hu/api/publication/34320436},
	author = {Nghi, Hoang Thao and Shahmohammadi, Sayeh and Ebrahimi, Kourosh H.},
	doi = {10.1016/j.cbpa.2023.102338},
	journal-iso = {CURR OPIN CHEM BIOL},
	journal = {CURRENT OPINION IN CHEMICAL BIOLOGY},
	volume = {76},
	unique-id = {34320436},
	issn = {1367-5931},
	abstract = {Inorganic complexes of iron and sulfur, that is, iron-sulfur [FeS] clusters, have played a fundamental role in life on Earth since the prebiotic period. These clusters were involved in elemen-tary reactions leading to the emergence of life and, since then, gained function in processes, such as respiration, replication, transcription, and the immune response. We discuss how three [FeS] proteins involved in the innate immune response play a role in oncogene expression/function and oncometabolism. Our analysis highlights the importance of future research into understanding the [FeS] clusters' roles in cancer progression and proliferation. The outcomes of these studies will help identify new targets and develop new anticancer therapeutics.},
	keywords = {CANCER; Oncogene; IRON-SULFUR CLUSTERS; Oncometabolism; Redox imbal- ance},
	year = {2023},
	eissn = {1879-0402},
	orcid-numbers = {Shahmohammadi, Sayeh/0000-0001-7681-5458}
}

@article{MTMT:32741660,
	title = {Enantioselective high-performance liquid chromatographic separation of fluorinated ß- phenylalanine derivatives utilizing Cinchona alkaloid-based ion-exchanger chiral stationary phases. Enantioselective separation of fluorinated ß-phenylalanine derivatives},
	url = {https://m2.mtmt.hu/api/publication/32741660},
	author = {Németi, Gábor and Berkecz, Róbert and Shahmohammadi, Sayeh and Forró, Enikő and Lindner, Wolfgang and Péter, Antal and Ilisz, István},
	doi = {10.1016/j.chroma.2022.462974},
	journal-iso = {J CHROMATOGR A},
	journal = {JOURNAL OF CHROMATOGRAPHY A},
	volume = {1670},
	unique-id = {32741660},
	issn = {0021-9673},
	year = {2022},
	eissn = {1873-3778},
	orcid-numbers = {Németi, Gábor/0000-0001-7312-8353; Berkecz, Róbert/0000-0002-9076-2177; Shahmohammadi, Sayeh/0000-0001-7681-5458; Forró, Enikő/0000-0001-6796-3889; Ilisz, István/0000-0001-8282-457X}
}

@article{MTMT:32787510,
	title = {Green Strategies for the Preparation of Enantiomeric 5–8-Membered Carbocyclic β-Amino Acid Derivatives through CALB-Catalyzed Hydrolysis},
	url = {https://m2.mtmt.hu/api/publication/32787510},
	author = {Shahmohammadi, Sayeh and Faragó, Tünde and Palkó, Márta and Forró, Enikő},
	doi = {10.3390/molecules27082600},
	journal-iso = {MOLECULES},
	journal = {MOLECULES},
	volume = {27},
	unique-id = {32787510},
	issn = {1431-5157},
	year = {2022},
	eissn = {1420-3049},
	orcid-numbers = {Shahmohammadi, Sayeh/0000-0001-7681-5458; Faragó, Tünde/0000-0002-3052-8258; Palkó, Márta/0000-0002-8265-7377; Forró, Enikő/0000-0001-6796-3889}
}

@article{MTMT:32936379,
	title = {Macrocyclic glycopeptides- and derivatized cyclofructan-based chiral stationary phases for the enantioseparation of fluorinated ß-phenylalanine analogs},
	url = {https://m2.mtmt.hu/api/publication/32936379},
	author = {Tanács, Dániel and Berkecz, Róbert and Shahmohammadi, Sayeh and Forró, Enikő and Armstrong, Daniel W. and Péter, Antal and Ilisz, István},
	doi = {10.1016/j.jpba.2022.114912},
	journal-iso = {J PHARMACEUT BIOMED ANAL},
	journal = {JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS},
	volume = {219},
	unique-id = {32936379},
	issn = {0731-7085},
	year = {2022},
	eissn = {1873-264X},
	orcid-numbers = {Tanács, Dániel/0000-0003-1011-8638; Berkecz, Róbert/0000-0002-9076-2177; Shahmohammadi, Sayeh/0000-0001-7681-5458; Forró, Enikő/0000-0001-6796-3889; Ilisz, István/0000-0001-8282-457X}
}

@CONFERENCE{MTMT:33551486,
	title = {Liquid Chromatographic Enantioseparation of Fluorinated ß-Phenylalanine Analogs Utilizing Superficially Porous Particles},
	url = {https://m2.mtmt.hu/api/publication/33551486},
	author = {Tanács, Dániel and Berkecz, Róbert and Shahmohammadi, Sayeh and Forró, Enikő and Daniel, W. Armstrong and Péter, Antal and Ilisz, István},
	booktitle = {33rd International Symposium on Chromatography – ISC 2022},
	unique-id = {33551486},
	year = {2022},
	orcid-numbers = {Tanács, Dániel/0000-0003-1011-8638; Berkecz, Róbert/0000-0002-9076-2177; Shahmohammadi, Sayeh/0000-0001-7681-5458; Forró, Enikő/0000-0001-6796-3889; Ilisz, István/0000-0001-8282-457X}
}

@CONFERENCE{MTMT:33672957,
	title = {Green enzymatic strategies for the preparation of enantiomeric carbocyclic beta-amino acid derivatives},
	url = {https://m2.mtmt.hu/api/publication/33672957},
	author = {Shahmohammadi, Sayeh and Faragó, Tünde and Palkó, Márta and Forró, Enikő},
	booktitle = {GreenCat 2022 Book of Abstracts},
	unique-id = {33672957},
	year = {2022},
	orcid-numbers = {Shahmohammadi, Sayeh/0000-0001-7681-5458; Faragó, Tünde/0000-0002-3052-8258; Palkó, Márta/0000-0002-8265-7377; Forró, Enikő/0000-0001-6796-3889}
}

@mastersthesis{MTMT:34118001,
	title = {New enzymatic strategies for the preparation of pharmaceutically important enantiomeric β-amino acid derivatives},
	url = {https://m2.mtmt.hu/api/publication/34118001},
	isbn = {9798381082999},
	author = {Shahmohammadi, Sayeh},
	doi = {10.14232/phd.11328},
	publisher = {Universití of Szeged},
	unique-id = {34118001},
	abstract = {The present Ph.D. work has been planned to accomplish two major goals. In view of the significance of fluorine-substituted compounds, the first aim was to synthesize a selection of (±)-β-amino carboxylic ester hydrochloride salts 3a–e, then to generate an appropriate lipase-catalyzed method for their resolution through hydrolysis, furnishing enantiopure new β-fluorophenyl-substituted β-amino acids (S)-5a–e and unreacted β-amino esters (R)-4a–e. The second objective of my work was a comparative investigation of different green strategies and then to build an environmentally benign CALB-catalyzed hydrolysis of cis carbocyclic amino esters 6–9.},
	year = {2022},
	orcid-numbers = {Shahmohammadi, Sayeh/0000-0001-7681-5458}
}

@article{MTMT:31862790,
	title = {Efficient Synthesis of New Fluorinated β-Amino Acid Enantiomers through Lipase-Catalyzed Hydrolysis},
	url = {https://m2.mtmt.hu/api/publication/31862790},
	author = {Shahmohammadi, Sayeh and Fülöp, Ferenc and Forró, Enikő},
	doi = {10.3390/molecules25245990},
	journal-iso = {MOLECULES},
	journal = {MOLECULES},
	volume = {25},
	unique-id = {31862790},
	issn = {1431-5157},
	year = {2020},
	eissn = {1420-3049},
	orcid-numbers = {Shahmohammadi, Sayeh/0000-0001-7681-5458; Fülöp, Ferenc/0000-0003-1066-5287; Forró, Enikő/0000-0001-6796-3889}
}