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Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/57971
Title: Convenient methods for the synthesis of a library of hemilabile phosphines
Authors: Jiménez, M. Victoria; Pérez-Torrente, Jesús J.; Bartolomé, M. Isabel; Oro, Luis A.
Issue Date: 2009
Publisher: Thieme
Citation: Synthesis 11: 1916-1922 (2009)
Abstract: A series of novel functionalized phosphines of hemilabile character, R 2P(CH2)nZ, have been prepared from diarylphosphines using several synthetic methodologies. The synthetic methods include the alkylation of lithium diarylphosphide or (diarylphosphino) borane adducts with functionalized halogenoalkanes, X(CH2)nZ, and the photochemical hydrophosphination of suitable functionalized allyl or vinyl derivatives, H2C=CHZ or H2C=CHCH2Z, using white light. A range of R2PH (R = Bn, 4-MeOC6H4, 4-MeC6H4, 2-MeC6H4, Ph, 4-F 3CC6H4) has been used in order to tune the electronic density on the phosphorus donor atom. The coordination ability of the hemilabile fragment was modified by selection of the donor group (Z = OMe, OEt, OBu, NMe2) or the length of the flexible carbon chain (n = 2, 3). Hemilabile fluorinated allylphosphines, R2PCH2CH=CH 2 (R = 4-FC6H4, C6F5), have been prepared from diarylchlorophosphines and allylmagnesium bromide. © Georg Thieme Verlag Stuttgart.
Publisher version (URL): http://dx.doi.org/10.1055/s-0028-1088060
URI: http://hdl.handle.net/10261/57971
DOI: 10.1055/s-0028-1088060
Identifiers: issn: 0039-7881
e-issn: 1437-210X
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