Facial selectivity in the Diels–Alder reactions of cis-cyclohexa-3,5-diene-1,2-diol and derivatives with N-phenylmaleimide
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Molecular Medicine
Link
http://pubs.rsc.org/en/content/articlepdf/1989/C3/C39890001439
Cited by 42 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. High-Pressure-Promoted and Facially Selective Diels–Alder Reactions of Enzymatically Derived cis-1,2-Dihydrocatechols and Their Acetonide Derivatives: Enantiodivergent Routes to Homochiral and Polyfunctionalized Bicyclo[2.2.2]octenes;The Journal of Organic Chemistry;2020-09-11
2. An approach to “escape from flatland”: chemo-enzymatic synthesis and biological profiling of a library of bridged bicyclic compounds;Organic & Biomolecular Chemistry;2016
3. Aza and oxo Diels–Alder reactions using cis-cyclohexadienediols of microbial origin: chemoenzymatic preparation of synthetically valuable heterocyclic scaffolds;Tetrahedron: Asymmetry;2015-12
4. Cycloreversion Approach For Preparation of Large π-Conjugated Compounds;Methods and Applications of Cycloaddition Reactions in Organic Syntheses;2014-01-10
5. Bent bonds and the antiperiplanar hypothesis as a simple model to predict Diels–Alder reactivity: retrospective or perspective?;Tetrahedron;2013-07
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