The diels-alder reaction of a 2,2-dimethoxyethyl ester via a cationic intermediate-Reference-Cited by-同舟云学术

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The diels-alder reaction of a 2,2-dimethoxyethyl ester via a cationic intermediate

Published:1990 Issue:39 Volume:31 Page:5625-5628
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Hashimoto Yukihiko,Saigo Kazuhiko,Machida Shigeru,Hasegawa Masaki

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference8 articles.

1. Facile Synthesis of Selectively Monoprotected Unsymmetrical 1,3-Diketones from 2,2-Dimethoxyethyl Esters

2. The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural Products

3. TRITYL PERCHLORATE AS AN EFFICIENT CATALYST IN THE ALDOL-TYPE REACTION

4. Trityl Salt Catalyzed Aldol Reaction between α,β-Acetylenic Ketones and Silyl Enol Ethers

Cited by 14 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: The Diels-Alder Reaction of a 2,2-Dimethoxyethyl Ester via a Cationic Intermediate.;ChemInform;2010-08-22

2. Acrylic Acid;Encyclopedia of Reagents for Organic Synthesis;2008-03-14

3. Titanium(IV) Chloride;Encyclopedia of Reagents for Organic Synthesis;2007-03-15

4. Trimethylsilyl Trifluoromethanesulfonate;Encyclopedia of Reagents for Organic Synthesis;2006-09-15

5. Methyl Acrylate;Encyclopedia of Reagents for Organic Synthesis;2006-04-15

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