Concentration Effect on the Stereoselectivity of [4+2] Cycloaddition Reactions of 3-Cyano-g-benzopyrone Derivatives with Electron Rich Dienes
Author:
Publisher
The Japan Institute of Heterocyclic Chemistry
Subject
Organic Chemistry,Pharmacology,Analytical Chemistry
Cited by 18 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. A Formal [3+3] Cycloaddition Approach To Natural Product Synthesis;Methods and Applications of Cycloaddition Reactions in Organic Syntheses;2014-01-10
2. ChemInform Abstract: Concentration Effect on the Stereoselectivity of [4 + 2] Cycloaddition Reactions of 3-Cyano-γ-benzopyrone Derivatives with Electron Rich Dienes.;ChemInform;2010-06-20
3. Intermolecular Cyclization Reactions to form Carbocycles;PATAI'S Chemistry of Functional Groups;2009-12-15
4. Strategies and approaches for constructing 1-oxadecalins;Tetrahedron;2006-11
5. Chemistry of 4-oxo-4H-1-benzopyran-3-carbonitrile;Journal of Heterocyclic Chemistry;2005-09
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