NDLI: Stable preformed chiral palladium catalysts for the one-pot asymmetric reductive amination of ketones.

Content Provider	Semantic Scholar
Author	Rubio-Pérez, Laura Pérez-Flores, Francisco Javier Sharma, Pankaj Velasco, L. Cabrera, Armando Capote
Copyright Year	2009
Abstract	The application of air stable preformed [(R)-BINAP]PdBr2, [(S)-BINAP]PdBr2, [(R)-Tol-BINAP]PdBr2, and [(S,S)-CHIRAPHOS]PdBr2 complexes in the one-pot asymmetric reductive amination of various carbonyl compounds, leading to chiral amines in very good yields with high enantioselectivities (<99% ee), is reported.
Starting Page	35
Ending Page	564
Page Count	530
File Format	PDF HTM / HTML
Alternate Webpage(s)	http://www.lac.dicp.ac.cn/pdf1/Pd/5.pdf
PubMed reference number	19093803v1
Alternate Webpage(s)	https://doi.org/10.1021/ol802336m
DOI	10.1021/ol802336m
Journal	Organic letters
Volume Number	11
Issue Number	2
Language	English
Access Restriction	Open
Subject Keyword	Amination Amines Ethinyl Estradiol Ketone Measurement Marijuana Abuse Palladium carbonyl compound
Content Type	Text
Resource Type	Article

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Stable preformed chiral palladium catalysts for the one-pot asymmetric reductive amination of ketones.