Base-Stimulated 1,2-, 1,4-, and 1,6-Eliminations in Suitably Substituted Alkylidenesuccinates Leading to Natural and Unnatural Conjugated Alkenyl(methyl)maleic Anhydrides
Author:
Affiliation:
1. Division of Organic Chemistry, National Chemical Laboratory (CSIR), Pune 411 008, India
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo402857r
Reference59 articles.
1. Natural Products with Maleic Anhydride Structure: Nonadrides, Tautomycin, Chaetomellic Anhydride, and Other Compounds
2. A Double Diastereoselective Michael-Type Addition as an Entry to Conformationally Restricted Tn Antigen Mimics
3. Highly Chemoselective Rauhut–Currier Reaction between Maleimides and Enones and Dual Phosphine-Mediated One-Pot Synthesis of Bicyclic and Polycyclic Skeletons
4. One-Step Synthesis of Complex Nitrogen Heterocycles from Imines and Alkyl-Substituted Maleic Anhydrides
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