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Controllable synthesis of P-chiral 1,2- and 1,3-diphosphines viaasymmetric DielsâAlder 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
- 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 DielsâAlder 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