Literature DB >> 18752225

Broader, greener, and more efficient: recent advances in asymmetric transfer hydrogenation.

Chao Wang1, Xiaofeng Wu, Jianliang Xiao.   

Abstract

Asymmetric transfer hydrogenation has become a practically useful tool in reduction chemistry in the last decade or so. This was largely triggered by the seminal work of Noyori and co-workers in the mid-1990s and is driven by its complementing chemistry to hydrogenation employing H(2). This Focus Review attempts to present a "holistic" overview on the advances in the area, focusing on the achievements recorded around the last three years. These include more-efficient and "greener" metal catalysts, catalysts that enable hydrogenation as well as transfer hydrogenation, biomimetic and organocatalysts, and their applications in the reduction of C==O, C==N, and C==C bonds. Also highlighted are efforts in the development of environmentally benign and reusable catalytic systems.

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Year:  2008        PMID: 18752225     DOI: 10.1002/asia.200800196

Source DB:  PubMed          Journal:  Chem Asian J        ISSN: 1861-471X


  11 in total

1.  Kinetic resolution of secondary alcohols using amidine-based catalysts.

Authors:  Ximin Li; Hui Jiang; Eric W Uffman; Lei Guo; Yuhua Zhang; Xing Yang; Vladimir B Birman
Journal:  J Org Chem       Date:  2012-02-09       Impact factor: 4.354

2.  Transient Ru-methyl formate intermediates generated with bifunctional transfer hydrogenation catalysts.

Authors:  Richard H Perry; Kristen R Brownell; Konstantin Chingin; Thomas J Cahill; Robert M Waymouth; Richard N Zare
Journal:  Proc Natl Acad Sci U S A       Date:  2012-02-06       Impact factor: 11.205

Review 3.  Stable cyclic carbenes and related species beyond diaminocarbenes.

Authors:  Mohand Melaimi; Michèle Soleilhavoup; Guy Bertrand
Journal:  Angew Chem Int Ed Engl       Date:  2010-11-15       Impact factor: 15.336

4.  Reducing Challenges in Organic Synthesis with Stereoselective Hydrogenation and Tandem Catalysis.

Authors:  Patrick D Parker; Xintong Hou; Vy M Dong
Journal:  J Am Chem Soc       Date:  2021-04-23       Impact factor: 16.383

5.  Easy To Synthesize, Robust Organo-osmium Asymmetric Transfer Hydrogenation Catalysts.

Authors:  James P C Coverdale; Carlos Sanchez-Cano; Guy J Clarkson; Rina Soni; Martin Wills; Peter J Sadler
Journal:  Chemistry       Date:  2015-04-08       Impact factor: 5.236

6.  Enantio-relay catalysis constructs chiral biaryl alcohols over cascade Suzuki cross-coupling-asymmetric transfer hydrogenation.

Authors:  Dacheng Zhang; Xiaoshuang Gao; Tanyu Cheng; Guohua Liu
Journal:  Sci Rep       Date:  2014-05-28       Impact factor: 4.379

Review 7.  Opportunities offered by chiral η⁶-arene/N-arylsulfonyl-diamine-RuII catalysts in the asymmetric transfer hydrogenation of ketones and imines.

Authors:  Jiří Václavík; Petr Kačer; Marek Kuzma; Libor Cervený
Journal:  Molecules       Date:  2011-06-28       Impact factor: 4.411

8.  Boron Tetrafluoride Anion Bonding Dual Active Species Within a Large-Pore Mesoporous Silica for Two-Step Successive Organic Transformaion to Prepare Optically Pure Amino Alcohols.

Authors:  Liang Li; Dongfeng Yang; Zhongrui Zhao; Yongkang Song; Lei Zhao; Rui Liu; Guohua Liu
Journal:  Front Chem       Date:  2018-07-06       Impact factor: 5.221

9.  Cyclopentadienone Iron Tricarbonyl Complexes-Catalyzed Hydrogen Transfer in Water.

Authors:  Daouda Ndiaye; Sébastien Coufourier; Mbaye Diagne Mbaye; Sylvain Gaillard; Jean-Luc Renaud
Journal:  Molecules       Date:  2020-01-20       Impact factor: 4.411

10.  Sulfone Group as a Versatile and Removable Directing Group for Asymmetric Transfer Hydrogenation of Ketones.

Authors:  Vijyesh K Vyas; Guy J Clarkson; Martin Wills
Journal:  Angew Chem Int Ed Engl       Date:  2020-07-01       Impact factor: 15.336

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