Development of Highly Stereoselective Reactions Utilizing Heteroatoms : New Approach to the Stereoselective Horner-Wadsworth-Emmons Reaction
Author:
Publisher
Pharmaceutical Society of Japan
Subject
Pharmaceutical Science,Pharmacology
Link
https://www.jstage.jst.go.jp/article/yakushi1947/120/5/120_5_432/_pdf
Cited by 17 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
1. Z-Selective Horner–Wadsworth–Emmons reaction of 2-TOM-cyclopentanone for the synthesis of rac-N-Cbz-Gly-Ψ[(Z)-CF C]-Pro-OH dipeptide isostere;Tetrahedron Letters;2014-11
2. E-Selective Horner–Wadsworth–Emmons reaction of 2-OBO-cyclopentanone for the synthesis of rac-N-Cbz-Gly-Ψ[(E)-CFC]-Pro-OH dipeptide isostere;Tetrahedron Letters;2014-08
3. P-Acylphosphonium salts and their vinyloges — application in synthesis;Open Chemistry;2010-12-01
4. ChemInform Abstract: Development of Highly Stereoselective Reactions Utilizing Heteroatoms. New Approach to the Stereoselective Horner-Wadsworth-Emmons Reaction;ChemInform;2010-06-03
5. Tandem reduction–olefination of triethyl 2-acyl-2-fluoro-2-phosphonoacetates and a synthetic approach to Cbz-Gly-Ψ[(Z)-CFC]-Gly dipeptide isostere;Tetrahedron;2006-12
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