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NMR assignment of absolute configuration of a P-chiral diphosphine and mechanics of its stereoselective formation

Abstract:
Two-dimensional rotating-frame nuclear Overhauser enhancement (ROESY) NMR spectra are used to determine the absolute configuration of (+)-diphenyl- phosphine-2,3-dimethyl-7-phenyl-7-phosphabicyclo[2.2.1]hept-2-ene. This diphosphine ligand is obtained from the palladium complex-promoted Diels- Alder reaction between diphenylvinylphosphine and 1-phenyl-3,3- dimethylphosphole in the presence of (R)-dimethyl(1-(α-naphthyl)ethylamine as the chiral auxiliary. The origin of the stereoselectivity in this asymmetric reaction is also revealed by solution NMR studies.
Publication status:
Published

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Publisher copy:
10.1016/0957-4166(96)00210-8

Authors

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Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Inorganic Chemistry
Role:
Author


Journal:
TETRAHEDRON-ASYMMETRY More from this journal
Volume:
7
Issue:
6
Pages:
1753-1762
Publication date:
1996-06-01
DOI:
ISSN:
0957-4166


Language:
English
Pubs id:
pubs:115951
UUID:
uuid:0dcbf8d0-f033-47eb-931c-13e306c3b486
Local pid:
pubs:115951
Source identifiers:
115951
Deposit date:
2012-12-19
ARK identifier:

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