Asymmetric synthesis and the novel retro Diels-Alder reaction of a P-chiral sulfonyl-substituted phosphanorbornene

Please use this identifier to cite or link to this item: https://doi.org/10.1016/S0957-4166(00)00219-6

Title:	Asymmetric synthesis and the novel retro Diels-Alder reaction of a P-chiral sulfonyl-substituted phosphanorbornene
Authors:	Leung, P.-H. Lang, H. Zhang, X. Selvaratnam, S. Vittal, J.J.
Issue Date:	14-Jul-2000
Citation:	Leung, P.-H., Lang, H., Zhang, X., Selvaratnam, S., Vittal, J.J. (2000-07-14). Asymmetric synthesis and the novel retro Diels-Alder reaction of a P-chiral sulfonyl-substituted phosphanorbornene. Tetrahedron Asymmetry 11 (13) : 2661-2664. ScholarBank@NUS Repository. https://doi.org/10.1016/S0957-4166(00)00219-6
Abstract:	An asymmetric Diels-Alder reaction between phenylvinylsulfone and 1-phenyl-3,4-dimethylphosphole in the presence of a chiral organometallic reaction promoter generates the corresponding P-chiral sulfonyl-substituted phosphanorbornene which is found to undergo the facile cycloreversion reaction under mild conditions. Copyright (C) 2000 Elsevier Science Ltd.
Source Title:	Tetrahedron Asymmetry
URI:	http://scholarbank.nus.edu.sg/handle/10635/75626
ISSN:	09574166
DOI:	10.1016/S0957-4166(00)00219-6
Appears in Collections:	Staff Publications

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