Literature DB >> 25428596

Enantioselective synthesis of benzoindolizidine derivatives using chiral phase-transfer catalytic intramolecular domino aza-Michael addition/alkylation.

Jiajia Guo1, Shouyun Yu.   

Abstract

An efficient and enantioselective strategy to synthesize benzoindolizidines from α,β-unsaturated amino ketones via domino intramolecular aza-Michael addition/alkylation was developed. These reactions were enabled by cinchona alkaloid-derived quaternary ammonium salts as the phase-transfer catalyst. A variety of benzoindolizidines were prepared in good yields (up to 93%) and enantioselectivities (up to 92.8:7.2 er).

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Year:  2014        PMID: 25428596     DOI: 10.1039/c4ob02227k

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  1 in total

1.  Diastereoselective auxiliary- and catalyst-controlled intramolecular aza-Michael reaction for the elaboration of enantioenriched 3-substituted isoindolinones. Application to the synthesis of a new pazinaclone analogue.

Authors:  Romain Sallio; Stéphane Lebrun; Frédéric Capet; Francine Agbossou-Niedercorn; Christophe Michon; Eric Deniau
Journal:  Beilstein J Org Chem       Date:  2018-03-09       Impact factor: 2.883

  1 in total

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