Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/57971
Título : Convenient methods for the synthesis of a library of hemilabile phosphines
Autor : Jiménez, M. Victoria, Pérez-Torrente, Jesús J., Bartolomé, M. Isabel, Oro, Luis A.
Fecha de publicación : 2009
Editor: Thieme
Citación : Synthesis 11: 1916-1922 (2009)
Resumen: 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.
URI : http://hdl.handle.net/10261/57971
Identificadores: doi: 10.1055/s-0028-1088060
issn: 0039-7881
e-issn: 1437-210X
Appears in Collections:(ICMA) Artículos

Files in This Item:
File Description SizeFormat 
accesoRestringido.pdf15,38 kBAdobe PDFView/Open
Show full item record
 
CSIC SFX LinksSFX Query

Items in Digital.CSIC are protected by copyright, with all rights reserved, unless otherwise indicated.