Literature DB >> 25563665

Asymmetric Kita spirolactonisation catalysed by anti-dimethanoanthracene-based iodoarenes.

Stephen J Murray1, Hasim Ibrahim.   

Abstract

Enantiopure C2-symmetric iodoarenes based on the rigid all-carbon anti-dimethanoanthracene framework are shown to catalyse the asymmetric oxidative Kita spirolactonisation of propanoic acid-tethered 1-naphthols with significant levels of asymmetric induction of up to 67% ee.

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Year:  2015        PMID: 25563665     DOI: 10.1039/c4cc09724f

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  4 in total

1.  Syntheses of arnottin I and arnottin II.

Authors:  Matthew J Moschitto; David R Anthony; Chad A Lewis
Journal:  J Org Chem       Date:  2015-03-09       Impact factor: 4.354

2.  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

3.  Catalytic asymmetric hydroxylative dearomatization of 2-naphthols: synthesis of lacinilene derivatives.

Authors:  Yu Zhang; Yuting Liao; Xiaohua Liu; Xi Xu; Lili Lin; Xiaoming Feng
Journal:  Chem Sci       Date:  2017-07-24       Impact factor: 9.825

4.  Construction of spirocarbocycles via gold-catalyzed intramolecular dearomatization of naphthols.

Authors:  Wen-Ting Wu; Ren-Qi Xu; Liming Zhang; Shu-Li You
Journal:  Chem Sci       Date:  2016-02-02       Impact factor: 9.825

  4 in total

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