Diastereoselective reactions of optically active γ-substituted vinyl phosphine oxides

Jonathan Clayden; Adam Nelson; Stuart Warren

doi:10.1016/S0040-4039(97)00658-8

Diastereoselective reactions of optically active γ-substituted vinyl phosphine oxides

Jonathan Clayden^*, Adam Nelson, Stuart Warren

^*Corresponding author for this work

School of Chemistry

Research output: Contribution to journal › Article (Academic Journal) › peer-review

20 Citations (Scopus)

Abstract

Dehydration of diphenylphosphinoyl diols (synthesised by asymmetric dihydroxylation of allylic phosphine oxides) gives γ-hydroxy vinyl phosphine oxides. Some diastereoselective reactions of vinyl phosphine oxides with hydrogen, carbon and heteroatomic nucleophiles are discussed.

Original language	English
Pages (from-to)	3471-3474
Number of pages	4
Journal	Tetrahedron Letters
Volume	38
Issue number	19
DOIs	https://doi.org/10.1016/S0040-4039(97)00658-8
Publication status	Published - 12 May 1997

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@article{cd97868fbfc94dbfa0dc350f65f82bdc,

title = "Diastereoselective reactions of optically active γ-substituted vinyl phosphine oxides",

abstract = "Dehydration of diphenylphosphinoyl diols (synthesised by asymmetric dihydroxylation of allylic phosphine oxides) gives γ-hydroxy vinyl phosphine oxides. Some diastereoselective reactions of vinyl phosphine oxides with hydrogen, carbon and heteroatomic nucleophiles are discussed.",

author = "Jonathan Clayden and Adam Nelson and Stuart Warren",

year = "1997",

month = may,

day = "12",

doi = "10.1016/S0040-4039(97)00658-8",

language = "English",

volume = "38",

pages = "3471--3474",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier",

number = "19",

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TY - JOUR

T1 - Diastereoselective reactions of optically active γ-substituted vinyl phosphine oxides

AU - Clayden, Jonathan

AU - Nelson, Adam

AU - Warren, Stuart

PY - 1997/5/12

Y1 - 1997/5/12

N2 - Dehydration of diphenylphosphinoyl diols (synthesised by asymmetric dihydroxylation of allylic phosphine oxides) gives γ-hydroxy vinyl phosphine oxides. Some diastereoselective reactions of vinyl phosphine oxides with hydrogen, carbon and heteroatomic nucleophiles are discussed.

AB - Dehydration of diphenylphosphinoyl diols (synthesised by asymmetric dihydroxylation of allylic phosphine oxides) gives γ-hydroxy vinyl phosphine oxides. Some diastereoselective reactions of vinyl phosphine oxides with hydrogen, carbon and heteroatomic nucleophiles are discussed.

UR - http://www.scopus.com/inward/record.url?scp=0030919222&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(97)00658-8

DO - 10.1016/S0040-4039(97)00658-8

M3 - Article (Academic Journal)

AN - SCOPUS:0030919222

SN - 0040-4039

VL - 38

SP - 3471

EP - 3474

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 19

ER -

Diastereoselective reactions of optically active γ-substituted vinyl phosphine oxides

Abstract

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