Efficient Procedure for the Reduction of α-Amino Acids to Enantiomerically Pure α-Methylamines
Author:
Affiliation:
1. Department of Chemical Sciences, Wyeth-Ayerst Research, Princeton, New Jersey 08543-8000 quaglid@war.wyeth.com
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo000242h
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1. Synthesis and hypoglycemic activity of N-alkylated hydrazonopropionic acids
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3. Conversion of chiral amino acids to enantiomerically pure α-methylamines
4. A Simple and Efficient Procedure for the Synthesis of Optically Active 4-Methoxy-α-Methylphenylethylamine from Tyrosine
5. LiBH4(NaBH4)/Me3SiCl, an Unusually Strong and Versatile Reducing Agent
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