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Controllable synthesis of P-chiral 1,2- and 1,3-diphosphines viaasymmetric Diels–Alder reactions involving functionalized allylic phosphines as dienophilesElectronic supplementary information (ESI) available: Syntheses of all the metal complexes, ligands and NMR data. CCDC reference numbers 711830 and 711831. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/b904090k

Authors :
Yuan, Mingjun
Pullarkat, Sumod A.
Yeong, Crystal Huixian
Li, Yongxin
Krishnan, Deepa
Pak-Leung, Hing
Source :
Dalton Transactions: An International Journal of Inorganic Chemistry. May2009, Vol. 2009 Issue 19, p3668-3670. 3p.
Publication Year :
2009

Abstract

Optically pure P-chiral 1,2- and 1,3-diphosphines were synthesized chemoselectively and stereoselectively from the chiral organopalladium complex promoted asymmetric Diels–Alder reaction between 3,4-dimethyl-1-phenylphosphole (DMPP) and cis- and trans-ester substituted allylic phosphines. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14779226
Volume :
2009
Issue :
19
Database :
Academic Search Index
Journal :
Dalton Transactions: An International Journal of Inorganic Chemistry
Publication Type :
Academic Journal
Accession number :
39058680
Full Text :
https://doi.org/10.1039/b904090k