Scinovex
reviewTop 1% cited

PhosphinooxazolinesA New Class of Versatile, Modular P,N<i>-</i>Ligands for Asymmetric Catalysis

Accounts of Chemical Research · 2000 · Vol. 33(6) · pp. 336–345
Günter HelmchenAndreas Pfaltz

Abstract

Chiral phosphinooxazolines (PHOX ligands), which coordinate to a metal center with a N- and a P-atom, allow effective enantiocontrol in a variety of metal-catalyzed reactions. They are readily synthesized, and because of their modular structure, the steric and electronic properties can be tailored for a specific application by variation of the oxazoline ring, the backbone, and the phosphine moiety.

Asymmetric Hydrogenation and CatalysisAsymmetric Synthesis and CatalysisSynthesis and Catalytic ReactionsMoietySteric effectsOxazolineChemistryRing (chemistry)Modular designPhosphineCombinatorial chemistryCatalysisStereochemistry

MeSH terms

CatalysisLigandsMolecular ConformationOrganometallic CompoundsOrganophosphorus CompoundsOxazolesPalladiumPhosphinesRubidiumStereoisomerism
Citations
1,293
FWCI
45.77
field-weighted impact
References
55
Percentile
100%
vs. same field & year
Citations per year
Cited by
Pd Asymmetric Allylic Alkylation (AAA). A Powerful Synthetic Tool.
Chemical and Pharmaceutical Bulletin · 2002 · 316 citations
Asymmetric hydrogenation of aromatic compounds
Organic & Biomolecular Chemistry · 2005 · 361 citations
Citation Network

How this paper connects to the literature. Drag to explore, click any node to open that paper.

PhosphinooxazolinesA New Class of Versatile, Modular P,N<i>-</i>Ligands for Asymmetric Catalysis · Scinovex