[4 + 2]-Annulations of Aminocyclobutanes
Author:
Affiliation:
1. Laboratory of Catalysis and Organic Synthesis, Ecole Polytechnique Fédérale de Lausanne, EPFL SB ISIC LCSO, BCH 4306, 1015 Lausanne, Switzerland
Funder
Schweizerische Nationalfonds zur Förderung der Wissenschaftlichen Forschung
Hoffman-La Roche
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.5b00149
Reference29 articles.
1. Diverse Cycloaddition Chemistry Leading to Overall Michael Addition in the Reactions of 1,1-Bis(dimethylamino)-2,2-difluoroethene with α,β-Unsaturated Aldehydes, Ketones, Esters, and Nitriles
2. 1-Amino-3-siloxy-1,3-butadienes: Highly Reactive Dienes for the Diels−Alder Reaction
3. Hetero Diels−Alder Reactions of 1-Amino-3-siloxy-1,3-butadienes under Strictly Thermal Conditions
4. An Efficient Approach to Aspidosperma Alkaloids via [4 + 2] Cycloadditions of Aminosiloxydienes: Stereocontrolled Total Synthesis of (±)-Tabersonine. Gram-Scale Catalytic Asymmetric Syntheses of (+)-Tabersonine and (+)-16-Methoxytabersonine. Asymmetric Syntheses of (+)-Aspidospermidine and (−)-Quebrachamine
5. The Catalytic Asymmetric Diels-Alder Reactions and Post-cycloaddition Reductive Transpositions of 1-Hydrazinodienes
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