HIGHLY DIASTEREOSELECTIVE REDUCTION OF NEW CHIRAL ALPHA-KETOAMIDES
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
- Appears in Collection
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