Amino acids and peptides. XX. Reduction of .ALPHA.-substituted .ALPHA.-diazo esters. Convenient synthesis of .ALPHA.-hydrazinocarboxylic acids and their derivatives from .ALPHA.-amino acids.
Author:
Publisher
Pharmaceutical Society of Japan
Subject
Drug Discovery,General Chemistry,General Medicine
Link
http://www.jstage.jst.go.jp/article/cpb1958/24/4/24_4_800/_pdf
Cited by 11 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
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2. Diazo Compounds as Electrophiles To React with 1,4-Dilithio-1,3-dienes: Efficient Synthesis of 1-Imino-pyrrole Derivatives;Organic Letters;2013-08-07
3. Efficient three-step sequence for the deamination of α-aminoesters. Application to the synthesis of CysLT1 antagonists;Tetrahedron Letters;2009-06
4. Electrophilic Amination of Carbanions, Enolates, and Their Surrogates;Organic Reactions;2009-03-16
5. New Entry for Synthesis of N-Acylhydrazones, Pyridazinones, and 1,3,4-Oxadiazin-6-ones from .ALPHA.-Amino Acid Esters;Chemical and Pharmaceutical Bulletin;2007
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