1990
DOI: 10.1080/10426509008038032
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PHOSPHINES SULFONEES ASYMETRIQUES V.ACINETIQUE DE SULFONATION DES PHOSPHINES

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Cited by 29 publications
(8 citation statements)
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“…DPPE-TS ( L38a ), DPPP-TS ( L38b ), and DPPB-TS ( L38c ) (Table ) have all been prepared by sulfonation of the corresponding 1,ω-bis(diphenylphosphino)alkanes using oleum. The rate of sulfonation increases as the alkyl bridge becomes longer (DPPE < DPPP < DPPB) presumably due to the deactivating effect of the neighboring phosphonium salt . Herrmann’s boric acid protocol was used to prepare L38b in 90% yield and 98% purity .…”
Section: Design Of Hydrophilic Ligandsmentioning
confidence: 99%
“…DPPE-TS ( L38a ), DPPP-TS ( L38b ), and DPPB-TS ( L38c ) (Table ) have all been prepared by sulfonation of the corresponding 1,ω-bis(diphenylphosphino)alkanes using oleum. The rate of sulfonation increases as the alkyl bridge becomes longer (DPPE < DPPP < DPPB) presumably due to the deactivating effect of the neighboring phosphonium salt . Herrmann’s boric acid protocol was used to prepare L38b in 90% yield and 98% purity .…”
Section: Design Of Hydrophilic Ligandsmentioning
confidence: 99%
“…Methylation occurred at positions 2, 3, or 6 and 1.8 OH groups per glucopyranose unit were statistically modified. DPPETS, 13a,21 DPPPTS 21 or DPPBTS 21 was prepared as reported in the literature. 22 The purity of these diphosphines was carefully controlled.…”
Section: Methodsmentioning
confidence: 99%
“…To circumvent these difficulties, an alternative is to introduce the oleum‐sensitive group after the sulfonation step. We propose herein a new methodology to access disulfonated alkyldiphenylphosphane from tetrasulfonated 1,2‐bis(diphenylphosphanyl)ethane (DPPETS)8,9 and an alkyl halide. The desired water‐soluble phosphanes can be obtained by alkylation then cleavage of DPPETS.…”
Section: Introductionmentioning
confidence: 99%