Lewis acid induced tandem carbocationic ring opening and cyclizations of α-[bis(methylthio)methylene]ethyl-2-styrylcyclopropyl ketones and carbinols: Novel approach to bicyclo[3.3.0]octene and cyclopent[a]indene frameworks-Reference-Cited by-同舟云学术

Lewis acid induced tandem carbocationic ring opening and cyclizations of α-[bis(methylthio)methylene]ethyl-2-styrylcyclopropyl ketones and carbinols: Novel approach to bicyclo[3.3.0]octene and cyclopent[a]indene frameworks

Published:1998-01 Issue:3-4 Volume:54 Page:531-540
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Patra Pranab K,Sriram V,Ila H,Junjappa H

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference41 articles.

1. Ketene Dithioacetals in Organic Synthesis: Recent Developments

2. α-Oxoketene-S,S-, N,S- and N,N-acetals: Versatile intermediates in organic synthesis

3. α-Oxoketene Dithioacetals as Intermediates for Aromatic Annelation

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

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