Literature DB >> 34759073

Synthesis and applications of high-performance P-chiral phosphine ligands.

Tsuneo Imamoto1.   

Abstract

Metal-catalyzed asymmetric synthesis is one of the most important methods for the economical and environmentally benign production of useful optically active compounds. The success of the asymmetric transformations is significantly dependent on the structure and electronic properties of the chiral ligands coordinating to the center metals, and hence the development of highly efficient ligands, especially chiral phosphine ligands, has long been an important research subject in this field. This review article describes the synthesis and applications of P-chiral phosphine ligands possessing chiral centers at the phosphorus atoms. Rationally designed P-chiral phosphine ligands are synthesized by the use of phosphine-boranes as the intermediates. Conformationally rigid and electron-rich P-chiral phosphine ligands exhibit excellent enantioselectivity and high catalytic activity in various transition-metal-catalyzed asymmetric reactions. Recent mechanistic studies of rhodium-catalyzed asymmetric hydrogenation are also described.

Entities:  

Keywords:  P-chiral phosphine ligand; asymmetric hydrogenation; catalytic asymmetric synthesis; enantioselection mechanism; phosphine–borane

Mesh:

Substances:

Year:  2021        PMID: 34759073      PMCID: PMC8610783          DOI: 10.2183/pjab.97.026

Source DB:  PubMed          Journal:  Proc Jpn Acad Ser B Phys Biol Sci        ISSN: 0386-2208            Impact factor:   3.493


  48 in total

1.  Applications and stereoselective syntheses of P-chirogenic phosphorus compounds.

Authors:  Mathieu Dutartre; Jérôme Bayardon; Sylvain Jugé
Journal:  Chem Soc Rev       Date:  2016-08-01       Impact factor: 54.564

2.  1-tert-butyl-2-methylphospholane-borane and its coupling product 2,2'-bis(1-tert-butylphospholane-borane)

Authors: 
Journal:  Acta Crystallogr C       Date:  2000-06       Impact factor: 1.172

3.  P-Chiral Phosphorus Ligands Based on a 2,3-Dihydrobenzo[ d][1,3]oxaphosphole Motif for Asymmetric Catalysis.

Authors:  Guangqing Xu; Chris H Senanayake; Wenjun Tang
Journal:  Acc Chem Res       Date:  2019-03-08       Impact factor: 22.384

4.  Stereoselective synthesis of o-bromo (or iodo)aryl P-chirogenic phosphines based on aryne chemistry.

Authors:  Jérôme Bayardon; Hugo Laureano; Vincent Diemer; Mathieu Dutartre; Utpal Das; Yoann Rousselin; Jean-Christophe Henry; Françoise Colobert; Frédéric R Leroux; Sylvain Jugé
Journal:  J Org Chem       Date:  2012-06-27       Impact factor: 4.354

5.  Asymmetric hydrogenation of enamides with Rh-BisP and Rh-miniPHOS catalysts. scope, limitations, and mechanism.

Authors:  I D Gridnev; M Yasutake; N Higashi; T Imamoto
Journal:  J Am Chem Soc       Date:  2001-06-06       Impact factor: 15.419

6.  Interconversion of monohydride intermediates in Rh(I)-catalyzed asymmetric hydrogenation of dimethyl 1-benzoyloxyethenephosphonate.

Authors:  I D Gridnev; N Higashi; T Imamoto
Journal:  J Am Chem Soc       Date:  2001-05-16       Impact factor: 15.419

7.  Direct enantio-convergent transformation of racemic substrates without racemization or symmetrization.

Authors:  Hajime Ito; Shun Kunii; Masaya Sawamura
Journal:  Nat Chem       Date:  2010-08-29       Impact factor: 24.427

8.  Marked deuterium isotope effects on the enantioselectivity in rhodium-catalyzed asymmetric hydrogenation of enamides.

Authors:  Tsuneo Imamoto; Takuma Itoh; Kazuhiro Yoshida; Ilya D Gridnev
Journal:  Chem Asian J       Date:  2008-09-01

9.  Enantioselective Allylation Using Allene, a Petroleum Cracking Byproduct.

Authors:  Richard Y Liu; Yujing Zhou; Yang Yang; Stephen L Buchwald
Journal:  J Am Chem Soc       Date:  2019-02-01       Impact factor: 15.419

10.  Computational design of high-performance ligand for enantioselective Markovnikov hydroboration of aliphatic terminal alkenes.

Authors:  Hiroaki Iwamoto; Tsuneo Imamoto; Hajime Ito
Journal:  Nat Commun       Date:  2018-06-12       Impact factor: 14.919

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  1 in total

1.  Enantioselective hydrogen-bond-donor catalysis to access diverse stereogenic-at-P(V) compounds.

Authors:  Katherine C Forbes; Eric N Jacobsen
Journal:  Science       Date:  2022-06-09       Impact factor: 63.714

  1 in total

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