One-carbon ring-expansion of 2-substituted cyclohexanones via lithium- and magnesium β-oxido carbenoid rearrangement: a new synthesis of 2,7-disubstituted and 2,2,7-trisubstituted cycloheptanones-Reference-Cited by-同舟云学术

One-carbon ring-expansion of 2-substituted cyclohexanones via lithium- and magnesium β-oxido carbenoid rearrangement: a new synthesis of 2,7-disubstituted and 2,2,7-trisubstituted cycloheptanones

Published:2006-09 Issue:38 Volume:47 Page:6769-6773
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Satoh Tsuyoshi,Tanaka Shu,Asakawa Naoyuki

Funder

University of Tokyo

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference21 articles.

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2. Ring Enlargement in Organic Chemistry;Hesse,1991

3. Free radical-mediated ring expansion and related annulations

4. Nouvelle transposition de carbénoïdes lithiens α-alcoolates: synthèse régiospécifique de α-chlorocétones

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