Acid catalyzed ring opening of α-bis(methylthio)methylenealkyl cyclopropyl ketones: An intramolecular alkylation approach to substituted cyclopentanones-Reference-Cited by-同舟云学术

Acid catalyzed ring opening of α-bis(methylthio)methylenealkyl cyclopropyl ketones: An intramolecular alkylation approach to substituted cyclopentanones

Published:1988 Issue:17 Volume:29 Page:2111-2114
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Deb B,Asokan C.V,Ila H,Junjappa H

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference21 articles.

1. A simple synthesis of (±)-cedrene and (±)-cedrol using a synchronous double annulation process

2. Studies on the acid-catalyzed opening of non-rigid: acylcyclopropanes: a dramatic solvent effect. A route to the bicyclo[2.2.1]heptane ring system

3. Aryl participation in concerted cyclization of cyclopropyl ketones

4. Six-membered rings via olefin participation in the opening of acylcyclopropanes

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4. Cyclization and Cycloaddition Reactions of Cyclopropyl Carbonyls and Imines;Synthesis;2009-09-08

5. Synthesis of novel 3-arylcyclopenta[c]quinolines via acid-induced domino cyclization of 2-arylamino-2-methylthioethenyl 2-arylcyclopropyl ketones;Arkivoc;2007-01-25