Facile and efficient conjugate additions of β-dicarbonyl compounds and nitroalkanes to 4-aryl-4-oxobut-2-enoates-Reference-Cited by-同舟云学术

Facile and efficient conjugate additions of β-dicarbonyl compounds and nitroalkanes to 4-aryl-4-oxobut-2-enoates

Published:2011 Issue:7 Volume:76 Page:947-954
ISSN:0352-5139
Container-title:Journal of the Serbian Chemical Society
language:en
Short-container-title:JSCS

Author:

Lv Xin¹,Zhang Yaohong¹,Zhou Liejin¹,Wang Xiaoxia¹

Affiliation:

1. Zhejiang Key Laboratory for Reactive Chemistry on Solid Surfaces, College of Chemistry and Life Sciences, Zhejiang Normal University, Jinhua, P. R. China

Abstract

Facile and efficient conjugate additions of carbon nucleophiles, such as ?-dicarbonyl compounds and nitroalkanes, to 4-aryl-4-oxobut-2-enoates have been achieved under simple base catalysis. A variety of multi-functional ?-keto esters could be conveniently obtained in good to excellent yields with complete regioselectivity.

Publisher

National Library of Serbia

Subject

General Chemistry

Reference18 articles.

1. Construction of Quaternary Stereocenters: New Perspectives through Enantioselective Michael Reactions

2. Enantioselective Conjugate Additions

3. Conjugate Additions of Nitroalkanes to Electron-Poor Alkenes: Recent Results

4. Michael Adducts-Source for Biologically Potent Heterocycles

5. Dipeptidomimetic Ketomethylene Isosteres as Pro-moieties for Drug Transport via the Human Intestinal Di-/Tripeptide Transporter hPEPT1: Design, Synthesis, Stability, and Biological Investigations

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