Controllable synthesis of P-chiral 1,2- and 1,3-diphosphines via asymmetric Diels–Alder reactions involving functionalized allylic phosphines as dienophiles-Reference-Cited by-同舟云学术

Controllable synthesis of P-chiral 1,2- and 1,3-diphosphines via asymmetric Diels–Alder reactions involving functionalized allylic phosphines as dienophiles

Published:2009 Issue:19 Volume: Page:3668
ISSN:1477-9226
Container-title:Dalton Transactions
language:en
Short-container-title:Dalton Trans.

Author:

Yuan Mingjun,Pullarkat Sumod A.,Yeong Crystal Huixian,Li Yongxin,Krishnan Deepa,Leung Pak-Hing

Publisher

Royal Society of Chemistry (RSC)

Subject

Inorganic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2009/DT/B904090K

Reference12 articles.

1. Asymmetric Synthesis and Organometallic Chemistry of Functionalized Phosphines Containing Stereogenic Phosphorus Centers

2. Asymmetric synthesis of a rigid diphosphine ligand containing two phosphorus and four carbon stereogenic centres by means of a chiral palladium complex promoted Diels–Alder reaction

3. Asymmetric Synthesis of P-Chiral Diphosphines. Steric Effects on the Palladium-Complex-Promoted Asymmetric Diels−Alder Reaction between a Dimethylphenylphosphole and (E/Z)-Methyl-Substituted Diphenylvinylphosphines

4. A simple route to an enantiomerically pure diphosphine ligand containing a phosphorus stereogenic centre.

5. A Palladium Complex Promoted Asymmetric Synthesis of a Novel P-Chiral Diphosphine Containing an Ester Functional Group

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