1,3-Dipolar cycloadditions of nonstabilized azomethine ylides to planar chalcones via regio- and stereoselective route: A three-component strategy-Reference-Cited by-同舟云学术

1,3-Dipolar cycloadditions of nonstabilized azomethine ylides to planar chalcones via regio- and stereoselective route: A three-component strategy

Published:2016-02-08 Issue:4 Volume:46 Page:293-308
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Gayen Biswajit¹,Banerji Avijit²,Dhara Kaliprasanna²

Affiliation:

1. Budge Budge Institute of Technology, Budge Budge, Kolkata, India

2. Centre of Advanced Studies on Natural Products including Organic Synthesis, Department of Chemistry, University College of Science and Technology, University of Calcutta, Kolkata, India

Funder

B. Gayen thanks the Council of Scientific and Industrial Research (CSIR), New Delhi, India, for the award of a senior research fellowship.

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/00397911.2015.1135954

Reference37 articles.

1. Araplysillins-I and-II: Biologically active dibromotyrosine derivatives from the spongePsammaplysilla arabica

2. A simple procedure for determining the aqueous half-lives of pyrrolic metabolites of pyrrolizidine alkaloids

3. Decarboxylative transamination. Mechanism and applications to the synthesis of heterocyclic compounds

4. A short dipolar cycloaddition approach to γ-lactam alkaloids from cynometra hankei

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