Lithium butylchalcogenolate induced Michael-aldol tandem sequence: easy and rapid access to highly functionalized organochalcogenides and unsaturated compounds-Reference-Cited by-同舟云学术

Lithium butylchalcogenolate induced Michael-aldol tandem sequence: easy and rapid access to highly functionalized organochalcogenides and unsaturated compounds

Published:2009-05 Issue:19 Volume:50 Page:2181-2184
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Keppler Artur F.,Gariani Rogério A.,Lopes Danilo G.,Comasseto João V.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference21 articles.

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3. Product Class 5: Alkanethiols;Comasseto,2008

4. A simple preparation of syn-NH-amide aldols and amide-Baylis–Hillman adducts via a Michael–aldol tandem process

5. Overcoming the Limitations of the Morita−Baylis−Hillman Reaction: A Rapid and General Synthesis of α-Alkenyl-β′-hydroxy Thioesters

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