A novel synthesis of cyclobutenecarboxylic acid from α-acetylcyclopentanone-Reference-Cited by-同舟云学术

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A novel synthesis of cyclobutenecarboxylic acid from α-acetylcyclopentanone

Published:1973 Issue:49 Volume:14 Page:4961-4962
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Takeda A.,Tsuboi S.,Sakai F.,Tanabe M.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference4 articles.

1. Allylic rearrangement. III. Favorskii-type rearrangemnt of the vinylogs of .alpha.-chloroacetones

2. This procedure to prepare 3-alken-2-ones from acetylacetone and α-halogenoaldehydes has been explored by one of us (A. T.) recently: A. Takeda and T. Uno, to be published.

Cited by 6 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. A convenient synthesis of olefins via deacylation reaction;Tetrahedron;2004-03

2. Chloral;Encyclopedia of Reagents for Organic Synthesis;2001-04-15

3. Revision of the structure of the reaction product of chloral with α-acetylcyclopentanone in the presence of base;Tetrahedron Letters;1983-01

4. Rearrangements in Carbanions;Organic Chemistry: A Series of Monographs;1980

5. The mechanism of the alkaline rearrangement of 1,1,1-trichloro-2-penten-4-one;Tetrahedron Letters;1976-12

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