Intramolecular [2 + 2] cycloaddition reactions of vinylketenes. stereo- and regiospecific preparation of vinylketenes from α,β-unsaturated acid chlorides.-Reference-Cited by-同舟云学术

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Intramolecular [2 + 2] cycloaddition reactions of vinylketenes. stereo- and regiospecific preparation of vinylketenes from α,β-unsaturated acid chlorides.

Published:1985-01 Issue:46 Volume:26 Page:5619-5622
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Kulkarni Yashwant S.,Burbaum Beverly W.,Snider Barry B.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference18 articles.

1. Intramolecular [2 + 2] cycloadditions of ketenes

2. Intramolecular [2+2] cycloadditions of ketenes and keteniminium salts to olefins

3. Intramolecular [2 + 2] cycloadditions of ketenes. 2. Synthesis of chrysanthenone, .beta.-pinene, .beta.-cis-bergamotene, and .beta.-trans-bergamotene

4. Y.S. Kulkarni and B.B. Snider, unpublished results.

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2. Synthesis of Fused Indoline‐Cyclobutanone Derivatives via an Intramolecular [2+2] Cycloaddition;European Journal of Organic Chemistry;2019-04-12

3. Pericyclic Reactions;Organic Synthesis;2017

4. Cycloaddition and Electrocyclic Reactions of Vinylketenes, Allenylketenes, and Alkynylketenes;Organic Reactions;2015-07-24

5. The Synthesis of Monoterpenes 1980-1986;Total Synthesis of Natural Products;2007-02-20

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