A one-step, modular route to optically-active diphos ligands

E Louise Hazeland; Andy M Chapman; Paul G Pringle; Hazel A Sparkes

doi:10.1039/c5cc03517a

A one-step, modular route to optically-active diphos ligands

E Louise Hazeland, Andy M Chapman, Paul G Pringle, Hazel A Sparkes

School of Chemistry

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

6 Citations (Scopus)

475 Downloads (Pure)

Abstract

A chlorosilane elimination reaction has been developed that allows the efficient synthesis of optically pure C1-symmetric, C1-backboned diphosphines with a wide variety of stereoelectronic characteristics.

Original language	English
Number of pages	4
Journal	Chemical Communications
Volume	2015
Issue number	51
DOIs	https://doi.org/10.1039/c5cc03517a
Publication status	Published - 28 May 2015

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10.1039/c5cc03517a

A one-step, modular route to optically-active diphos ligandsFinal published version, 2.04 MB

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3-month Core Capability for Chemistry Research
Crosby, J. (Principal Investigator)
1/01/13 → 1/04/13
Project: Research

Professor Paul G Pringle
- Paul.Pringlebristol.acuk
- School of Chemistry - Professor of Inorganic Chemistry
Person: Academic

Cite this

@article{e22692b4ecec4f62b4cca6af550a9dfd,

title = "A one-step, modular route to optically-active diphos ligands",

abstract = "A chlorosilane elimination reaction has been developed that allows the efficient synthesis of optically pure C1-symmetric, C1-backboned diphosphines with a wide variety of stereoelectronic characteristics.",

author = "{Louise Hazeland}, E and Chapman, {Andy M} and Pringle, {Paul G} and Sparkes, {Hazel A}",

year = "2015",

month = may,

day = "28",

doi = "10.1039/c5cc03517a",

language = "English",

volume = "2015",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "51",

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T1 - A one-step, modular route to optically-active diphos ligands

AU - Louise Hazeland, E

AU - Chapman, Andy M

AU - Pringle, Paul G

AU - Sparkes, Hazel A

PY - 2015/5/28

Y1 - 2015/5/28

N2 - A chlorosilane elimination reaction has been developed that allows the efficient synthesis of optically pure C1-symmetric, C1-backboned diphosphines with a wide variety of stereoelectronic characteristics.

AB - A chlorosilane elimination reaction has been developed that allows the efficient synthesis of optically pure C1-symmetric, C1-backboned diphosphines with a wide variety of stereoelectronic characteristics.

U2 - 10.1039/c5cc03517a

DO - 10.1039/c5cc03517a

M3 - Article (Academic Journal)

C2 - 26017020

SN - 1359-7345

VL - 2015

JO - Chemical Communications

JF - Chemical Communications

IS - 51

ER -

A one-step, modular route to optically-active diphos ligands

Abstract

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3-month Core Capability for Chemistry Research

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Professor Paul G Pringle

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