Polyfunctional adducts assembled with the help of a one-pot sequence of three AdE reactions as synthetically useful intermediates. The course of the Lewis acid induced transformations of the 4,6-dialkoxy-7-arylthioheptene moiety
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference10 articles.
1. Controlled one-pot sequence of three AdE reactions as a novel protocol for the synthesis of polyfunctional compounds
2. Four-component couplingvia a sequence of threeAd E reactions involving arenesulfenyl chloride, two alkyl vinyl ether units, and silicon-containing π-donors as a method for the synthesis of polyfunctional compounds
3. Structure and reactivity of thiophanium salts, the elusive intermediates in ArS+-mediated one-pot sequence of three AdE reactions
4. Diastereoselective synthesis of polyfunctional compounds based on the tandem sequence of threeAd E reactions using cyclic vinyl ethers as first alkene components
5. Highly Stereoselective Cationic Cyclization Assisted by a Sulfenyl Group. Scope, Limitation, and Mechanism
Cited by 2 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. ChemInform Abstract: Polyfunctional Adducts Assembled with the Help of a One-Pot Sequence of Three AdE Reactions as Synthetically Useful Intermediates. The Course of the Lewis Acid Induced Transformations of the 4,6-Dialkoxy-7-arylthioheptene Moiety.;ChemInform;2010-05-24
2. Polyfunctional Compounds Containing the 4,6-Dialkoxy-7-arylthioheptene Moiety as Synthetically Useful Intermediates. The Course of Lewis Acid-Induced Transformations;The Journal of Organic Chemistry;2002-10-17
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