HIGHLY DIASTEREOSELECTIVE REDUCTION OF NEW CHIRAL ALPHA-KETOAMIDES

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Both pyruvamide and benzoylformamide having (S)-2-methoxymethylindoline as a chiral auxiliary were reduced with various reducing agents in high stereoselectivities (up to dr = 99 : 1).
Publisher
MARCEL DEKKER INC
Issue Date
1995
Language
English
Article Type
Article
Keywords

ASYMMETRIC-SYNTHESIS; KETO AMIDES; AMINO ACIDS; AUXILIARIES; ESTERS

Citation

SYNTHETIC COMMUNICATIONS, v.25, no.13, pp.1963 - 1969

ISSN
0039-7911
DOI
10.1080/00397919508015873
URI
http://hdl.handle.net/10203/72314
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