Highly Efficient Synthesis of Chiral β-Hydroxy Sulfides with High Enantiomeric Purity via CBS-Oxazaborolidine-Catalyzed Borane Reduction

Autor:	Byung Tae Cho, Ok Kyoung Choi, Dong Jun Kim
Rok vydání:	2002
Předmět:	Inorganic Chemistry Reduction (complexity) chemistry.chemical_compound Chemistry Organic Chemistry Organic chemistry General Medicine Physical and Theoretical Chemistry Enantiomer Borane Combinatorial chemistry Catalysis
Zdroj:	ChemInform. 33:94-94
ISSN:	0931-7597
DOI:	10.1002/chin.200240094
Popis:	A simple and efficient synthesis of chiral β-hydroxy p -tolylsulfides with high enantiomeric purity by CBS-oxazaborolidine-catalyzed asymmetric borane reduction of β-keto p -tolylsulfides using N -ethyl- N -isopropylaniline–borane complex as the borane carrier is reported.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::808c69be9c9695e6d23894a7addd9dbc https://doi.org/10.1002/chin.200240094 Zobrazit plný text záznamu Plný text