Enantioselective reduction of prochiral ketones by chromium(II) complexes with amino acid ligands as the source of chirality

Autor:	Tamás Patonay, Claudia Zucchi, József Jekő, Albert Lévai, Károly Micskei, Csongor Hajdu
Rok vydání:	1999
Předmět:	chemistry.chemical_classification Chromium Chemistry Stereochemistry Organic Chemistry Drug Discovery Enantioselective synthesis chemistry.chemical_element Chirality (chemistry) Biochemistry Amino acid
Zdroj:	Tetrahedron Letters. 40:1373-1374
ISSN:	0040-4039
DOI:	10.1016/s0040-4039(98)02611-2
Popis:	Prochiral ketones were reduced to enantiomerically enriched secondary alcohols by Cr(II)[L-amino acid] complexes in good yields and moderate enantioselectivity.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::ed3a54a3f92165775997a3132e7c0d1a https://doi.org/10.1016/s0040-4039(98)02611-2 Zobrazit plný text záznamu Full Text from ScienceDirect