Rearrangement of Spirocyclic Oxindoles with Lithium Amide Bases
Author:
Affiliation:
1. University Bordeaux 1, Institut des Sciences Moléculaires, UMR-CNRS 5255, 351, cours de la libération, 33405 Talence cedex 05, France, and University of Lausanne, Institut de Cristallographie, BCP, CH-1015 Dorigny-Lausanne, Switzerland
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol8016885
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1. Gelsemine: A Thought-Provoking Target for Total Synthesis
2. Total Synthesis of SR 121463 A, a Highly Potent and Selective Vasopressin V2 Receptor Antagonist
3. Facile synthesis of active antitubercular, cytotoxic and antibacterial agents: a Michael addition approach
4. Catalytic Asymmetric Synthesis of Quaternary Carbon Centers. Exploratory Investigations of Intramolecular Heck Reactions of (E)-α,β-Unsaturated 2-Haloanilides and Analogues To Form Enantioenriched Spirocyclic Products
5. New Spirocyclic Oxindole Synthesis Based on a Hetero Claisen Rearrangement
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