Literature DB >> 26449515

Chiral N,N'-Dioxide-Scandium(III)-Catalyzed Asymmetric Dearomatization of 2-Naphthols through an Amination Reaction.

Xiangjin Lian1, Lili Lin1, Guojin Wang1, Xiaohua Liu1, Xiaoming Feng2.   

Abstract

A catalytic asymmetric dearomatization of 2-naphthols with azodicarboxylates has been accomplished by using a N,N'-dioxide-scandium(III) complex as a chiral catalyst. A number of optically active β-naphthalenone compounds with a nitrogen-containing quaternary carbon stereocenter were obtained in up to 99 % yield and up to 99 % ee under mild reaction conditions. The reaction could be scaled up to a gram-scale with the yield and ee maintained. Based on these experiments and on previous reports, a possible transition state was proposed.
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  amination reaction; asymmetric catalysis; dearomatization; naphthols; scandium

Year:  2015        PMID: 26449515     DOI: 10.1002/chem.201503276

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  2 in total

1.  Chiral phosphoric acid catalyzed aminative dearomatization of α-naphthols/Michael addition sequence.

Authors:  Zi-Lei Xia; Chao Zheng; Ren-Qi Xu; Shu-Li You
Journal:  Nat Commun       Date:  2019-07-17       Impact factor: 14.919

2.  A Simple and Broadly Applicable C-N Bond Forming Dearomatization Protocol Enabled by Bifunctional Amino Reagents.

Authors:  Xiaofeng Ma; Joshua J Farndon; Tom A Young; Natalie Fey; John F Bower
Journal:  Angew Chem Int Ed Engl       Date:  2017-10-11       Impact factor: 15.336

  2 in total

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