Chiral Tricyclic Iminolactone Derived from (1R)-(+)-Camphor as a Glycine Equivalent for the Asymmetric Synthesis of α-Amino Acids-Reference-Cited by-同舟云学术

Chiral Tricyclic Iminolactone Derived from (1R)-(+)-Camphor as a Glycine Equivalent for the Asymmetric Synthesis of α-Amino Acids

Published:2002-03-09 Issue:7 Volume:67 Page:2309-2314
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Xu Peng-Fei¹,Chen Yuan-Shek¹,Lin Shu-I¹,Lu Ta-Jung¹

Affiliation:

1. College of Chemistry and Chemical Engineering, National Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou, Gansu 730000, PRC, and Department of Chemistry, National Chung-Hsing University, Taichung, Taiwan 40227, ROC

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo011139a

Reference37 articles.

1. New oxazinone and pyrazinone derivatives as chiral reagents for the asymmetric synthesis of α-amino acids

2. Catalytic Asymmetric Strecker Synthesis. Preparation of Enantiomerically Pure α-Amino Acid Derivatives from Aldimines and Tributyltin Cyanide or Achiral Aldehydes, Amines, and Hydrogen Cyanide Using a Chiral Zirconium Catalyst

3. New Expedient Route to Both Enantiomers of Nonproteinogenic α-Amino Acid Derivatives from the Unsaturated 2-Aza-Bicyclo Moiety

4. Acylnitrene Route to Vicinal Amino Alcohols. Application to the Synthesis of (−)-Bestatin and Analogues

5. Asymmetric synthesis of (S)-α-methyl α-amino acids by alkylation of chiral 3,6-dihydro-2H-1,4-oxazin-2-ones using unactivated alkyl halides and organic bases

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