Asymmetric synthesis of 2-substituted 4-chromanones using enzyme-catalyzed reactions

Autor:	Masashi Kawasaki, Chiho Hiraoka, Kanako Katayama, Naoki Toyooka, Akihisa Inoue, Akira Tanaka, Hiroko Kakuda, Michimasa Goto, Yuka Asano, Tadashi Kometani
Rok vydání:	2008
Předmět:	chemistry.chemical_classification biology Enzyme catalyzed Process Chemistry and Technology Enantioselective synthesis Bioengineering Optically active Biochemistry Esterase Catalysis Enzyme catalysis Hydrolysis Enzyme chemistry biology.protein Organic chemistry Lipase
Zdroj:	Journal of Molecular Catalysis B: Enzymatic. 54:93-102
ISSN:	1381-1177
DOI:	10.1016/j.molcatb.2007.12.022
Popis:	2-Substituted 4-chromanones were synthesized in their optically active forms. The chiral intermediates were obtained via lipase-catalyzed enantioselective reactions. Lipase and esterase were also used for the hydrolysis of ester moieties of the precursors of the target compounds under mild conditions.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::89126b7ffd6271506e76563c4b07a713 https://doi.org/10.1016/j.molcatb.2007.12.022 Zobrazit plný text záznamu Full Text from ScienceDirect