Literature DB >> 30762285

Spiro-Bicyclic Bisborane Catalysts for Metal-Free Chemoselective and Enantioselective Hydrogenation of Quinolines.

Xiang Li1, Jun-Jie Tian1, Ning Liu1, Xian-Shuang Tu1, Ning-Ning Zeng1, Xiao-Chen Wang1.   

Abstract

A new series of spiro-bicyclic bisborane catalysts has been prepared by means of hydroboration reactions of C2 -symmetric spiro-bicyclic dienes with HB(C6 F5 )2 and HB(p-C6 F4 H)2 . When used for hydrogenation of quinolines, these catalysts give excellent yields and enantiomeric excesses, and show turnover numbers of up to 460. The most attractive feature of these metal-free hydrogenation reactions was the broad functional-group tolerance, making this method complementary to existing methods for quinoline hydrogenation.
© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  asymmetric catalysis; boron; heterocycles; homogeneous catalysis; hydrogenation

Year:  2019        PMID: 30762285     DOI: 10.1002/anie.201900907

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


  2 in total

1.  Tunable and Cooperative Catalysis for Enantioselective Pictet-Spengler Reaction with Varied Nitrogen-Containing Heterocyclic Carboxaldehydes.

Authors:  Yuk-Cheung Chan; Marcus H Sak; Scott A Frank; Scott J Miller
Journal:  Angew Chem Int Ed Engl       Date:  2021-10-07       Impact factor: 15.336

2.  Iridium Complex-Catalyzed Transfer Hydrogenation of N-Heteroarenes and Tentative Asymmetric Synthesis.

Authors:  Lu Ouyang; Yanping Xia; Jianhua Liao; Rui Miao; Xiao Yang; Renshi Luo
Journal:  ACS Omega       Date:  2021-04-07
  2 in total

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