Literature DB >> 29577534

Transition-Metal-Free Decarboxylative Propargylic Substitution/Cyclization with either Azolium Enolates or Acyl Anions.

Shenci Lu1, Jun-Yang Ong1,2, Si Bei Poh1, Terence Tsang1, Yu Zhao1,2.   

Abstract

Presented herein is an unprecedented transition-metal-free propargylic substitution reaction with either azolium enolates or acyl anions, which are generated from aldehydes under N-heterocyclic carbene catalysis. This new catalytic activation operates on readily available cyclic propargylic carbamates through decarboxylation, and generates reactive allene intermediates that can undergo divergent cyclization pathways to deliver skeletally diverse polycyclic compounds with high levels of efficiency and excellent enantioselectivities.
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  N-heterocyclic carbenes; cycloaddition; decarboxylation; enantioselectivity; heterocycles

Year:  2018        PMID: 29577534     DOI: 10.1002/anie.201801340

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  3 in total

1.  A tandem dearomatization/rearomatization strategy: enantioselective N-heterocyclic carbene-catalyzed α-arylation.

Authors:  Zijun Wu; Jian Wang
Journal:  Chem Sci       Date:  2018-12-27       Impact factor: 9.825

2.  Two Catalytic Annulation Modes via Cu-Allenylidenes with Sulfur Ylides that Are Dominated by the Presence or Absence of Trifluoromethyl Substituents.

Authors:  Malla Reddy Gannarapu; Jun Zhou; Bingyao Jiang; Norio Shibata
Journal:  iScience       Date:  2020-03-20

Review 3.  An Update of Transition Metal-Catalyzed Decarboxylative Transformations of Cyclic Carbonates and Carbamates.

Authors:  Linhong Zuo; Teng Liu; Xiaowei Chang; Wusheng Guo
Journal:  Molecules       Date:  2019-10-31       Impact factor: 4.411

  3 in total

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