Highly Stereoselective Intramolecular Diels–Alder Reaction of Decatrienoates Activated byt-Butoxycarbonyl, Chloro, and Sulfonyl Groups at the Terminal Position-Reference-Cited by-同舟云学术

Highly Stereoselective Intramolecular Diels–Alder Reaction of Decatrienoates Activated byt-Butoxycarbonyl, Chloro, and Sulfonyl Groups at the Terminal Position

Published:2008-10-15 Issue:10 Volume:81 Page:1308-1314
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Inoue Seiichi,Yin Chunji,Kosugi Hiroko,Nabeta Atsuko,Sakai Yoko,Honda Kiyoshi,Hoshino Yujiro

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Reference33 articles.

1. The intramolecular Diels–Alder reaction: recent advances and synthetic applications

2. Aspects of the intramolecular Diels-Alder reactions of some 1,3,9-trienic amides, amines, and esters. An approach to the pentacyclic skeleton of the yohimboid alkaloids

3. Intramolecular Diels−Alder Reactions of Decatrienoates: Remote Stereocontrol and Conformational Activation1

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1. Formation of Alkenes by Diels-Alder Reactions;Comprehensive Organic Transformations;2018-02-28

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3. Tandem Wittig–intramolecular Diels–Alder cycloaddition of ester-tethered 1,3,9-decatrienes under microwave heating;Tetrahedron;2011-01

4. ChemInform Abstract: Highly Stereoselective Intramolecular Diels-Alder Reaction of Decatrienoates Activated by t-Butoxycarbonyl, Chloro, and Sulfonyl Groups at the Terminal Position.;ChemInform;2009-02-17

5. Remarkable rate acceleration of intramolecular Diels–Alder reaction in ionic liquids;Organic & Biomolecular Chemistry;2009