Highly enantio- and diastereoselective reduction of sulfur-functionalized cyclic ketones with baker's yeast

Autor:	Bingidimi I. Mobele, Kengo Yamanaka, Tamotsu Fujisawa, Makoto Shimizu
Rok vydání:	1991
Předmět:	Reduction (complexity) chemistry Organic Chemistry Drug Discovery Diastereomer Chemical reduction chemistry.chemical_element Organic chemistry Biochemistry Sulfur Yeast Enzyme catalysis Catalysis
Zdroj:	Tetrahedron Letters. 32:399-400
ISSN:	0040-4039
Popis:	Bakers' yeast reduction of 2-phenyltiocyclopentanone, 2-phenylthiocyclohexanone, and 2-phenylthio-2-cyclopentenone affords the corresponding (1S,2R)-2-phenylthiocycloalkanols in optically pure form and excellent diastereomeric excess.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::afaefd0ebb4128c3a08470648aff5c36 https://doi.org/10.1016/s0040-4039(00)92638-8 Zobrazit plný text záznamu