Literature DB >> 31638825

Copper-Catalyzed Asymmetric Propargylation of Indolizines.

Lei Yang1, Xiang Pu1, Dawen Niu1, Zhengyan Fu1, Xia Zhang1.   

Abstract

Methods to diversify indolizines are valuable for the discovery of medications and fluorescent molecules. The utilization of copper-catalyzed asymmetric propargylation to install a terminal alkyne handle on indolizine heterocycle is reported. This method delivers C3-propargylation products from C2-substituted indolizines or C1-propargylation products from C2,C3-disubstituted indolizines through a stereoconvergent pathway.

Entities:  

Year:  2019        PMID: 31638825     DOI: 10.1021/acs.orglett.9b03032

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  1 in total

1.  Enantioselective synthesis of α-tetrasubstituted (3-indolizinyl) (diaryl)methanamines via chiral phosphoric acid catalysis.

Authors:  Jialing Zhong; Rihuang Pan; Xufeng Lin
Journal:  RSC Adv       Date:  2022-07-15       Impact factor: 4.036

  1 in total

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