Literature DB >> 30211963

C2 -Symmetric Bicyclic Bisborane Catalysts: Kinetic or Thermodynamic Products of a Reversible Hydroboration of Dienes.

Xian-Shuang Tu1, Ning-Ning Zeng1, Ru-Ye Li1, Yu-Quan Zhao1, De-Zhen Xie1, Qian Peng1, Xiao-Chen Wang1.   

Abstract

We prepared a new class of chiral C2 -symmetric bicyclic bisborane catalysts by addition reactions of internal dienes with the Piers borane, HB(C6 F5 )2 , and an analogue, HB(p-C6 F4 H)2 . The dependence of the addition pattern on the reaction temperature allowed us to selectively prepare two diastereomeric catalysts from a single diene precursor. The bisboranes prepared in situ exhibited excellent activity (turnover numbers up to 200 at -40 °C) and enantioselectivity (up to 95 % ee) in imine hydrogenation reactions.
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  asymmetric catalysis; boron; frustrated Lewis pairs; homogeneous catalysis; hydrogenation

Year:  2018        PMID: 30211963     DOI: 10.1002/anie.201808289

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  2 in total

1.  Piers' Borane-Induced Tetramerization of Arylacetylenes.

Authors:  Max Hasenbeck; Tizian Müller; Arthur Averdunk; Jonathan Becker; Urs Gellrich
Journal:  Chemistry       Date:  2021-12-28       Impact factor: 5.020

2.  Aluminum-catalyzed tunable halodefluorination of trifluoromethyl- and difluoroalkyl-substituted olefins.

Authors:  Zhong Liu; Xian-Shuang Tu; Le-Tao Guo; Xiao-Chen Wang
Journal:  Chem Sci       Date:  2020-10-01       Impact factor: 9.825

  2 in total

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