» Articles » PMID: 10891054

Modular Phospholane Ligands in Asymmetric Catalysis

Overview
Journal Acc Chem Res
Specialty Chemistry
Date 2000 Jul 13
PMID 10891054
Citations 20
Authors
Affiliations
Soon will be listed here.
Abstract

This Account outlines the preparation and application of a class of phosphine ligands based upon the trans-2,5-disubstituted phospholane moiety. The modular nature of these ligands has allowed facile variation of both phospholane substituent and backbone structure, thus providing access to a series of ligands. Bidentate bis(phospholane) ligands have been found to be very useful in asymmetric catalytic hydrogenation reactions. In particular, we highlight the versatility of highly efficient bis(phospholane)rhodium catalysts that allow enantioselective hydrogenation to produce a diverse range of compounds containing C-N, C-O, and C-C stereogenic centers.

Citing Articles

Expedient and divergent synthesis of unnatural peptides through cobalt-catalyzed diastereoselective umpolung hydrogenation.

Song X, Bai S, Li Y, Yi T, Long X, Pu Q Sci Adv. 2023; 9(51):eadk4950.

PMID: 38117889 PMC: 10732522. DOI: 10.1126/sciadv.adk4950.


Trimerization and cyclization of reactive P-functionalities confined within OCO pincers.

Chinen B, Hyvl J, Brayton D, Riek M, Yoshida W, Chapp T RSC Adv. 2022; 11(46):28602-28613.

PMID: 35478534 PMC: 9038090. DOI: 10.1039/d1ra05926b.


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

Imamoto T Proc Jpn Acad Ser B Phys Biol Sci. 2021; 97(9):520-542.

PMID: 34759073 PMC: 8610783. DOI: 10.2183/pjab.97.026.


Desymmetrization Approach to the Synthesis of Optically Active P-Stereogenic Phosphin-2-en-4-ones.

Lastawiecka E, Frynas S, Pietrusiewicz K J Org Chem. 2021; 86(9):6195-6206.

PMID: 33900770 PMC: 8279496. DOI: 10.1021/acs.joc.0c03055.


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

Parker P, Hou X, Dong V J Am Chem Soc. 2021; 143(18):6724-6745.

PMID: 33891819 PMC: 9141585. DOI: 10.1021/jacs.1c00750.