Literature DB >> 28485600

Enantioselective Synthesis of 1,2-Dihydronaphthalenes via Oxidative N-Heterocyclic Carbene Catalysis.

Saima Perveen1, Zhifei Zhao1, Guoxiang Zhang1, Jian Liu1, Muhammad Anwar1, Xinqiang Fang1.   

Abstract

1,2-Dihydronaphthalenes are important molecules in both medicinal and synthetic chemistry, but methods for the catalytic asymmetric construction of this class of molecules are limited. The diastereo- and enantioselective N-heterocyclic carbene-catalyzed cascade annulation reactions using benzodiketones and enals under oxidative conditions, which afford a variety of 1,2-dihydronaphthalenes with two adjacent stereocenters in up to 99% yield, with >20:1 dr, and up to 99% ee, are reported. Furthermore, the product can be easily transformed to a series of useful compounds such as alcohol, amide, and epoxide.

Entities:  

Year:  2017        PMID: 28485600     DOI: 10.1021/acs.orglett.7b00555

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


  3 in total

1.  Iron-Catalyzed Synthesis of Tetrahydronaphthalenes via 3,4-Dihydro-2H-pyran Intermediates.

Authors:  Rebecca B Watson; Corinna S Schindler
Journal:  Org Lett       Date:  2017-12-20       Impact factor: 6.005

Review 2.  Recent advances of N-heterocyclic carbenes in the applications of constructing carbo- and heterocyclic frameworks with potential biological activity.

Authors:  Mei-Mei Li; Xiaozhen Chen; Yun Deng; Jun Lu
Journal:  RSC Adv       Date:  2021-11-26       Impact factor: 4.036

Review 3.  N-Heterocyclic-Carbene-Catalyzed Domino Reactions via Two or More Activation Modes.

Authors:  Xiang-Yu Chen; Sun Li; Fabrizio Vetica; Mukesh Kumar; Dieter Enders
Journal:  iScience       Date:  2018-04-05
  3 in total

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