Enantioselective rhodium-catalyzed addition of arylboronic acids to alkenylheteroarenes

Graham Pattison; Guillaume Piraux; Hon Wai Lam

doi:10.1021/ja106809p

Enantioselective rhodium-catalyzed addition of arylboronic acids to alkenylheteroarenes

Graham Pattison
, Guillaume Piraux
, Hon Wai Lam

Research output: Contribution to journal › Article › peer-review

Abstract

In the presence of a rhodium complex containing a newly developed chiral diene ligand, alkenes activated by a range of π-deficient or π-excessive heteroarenes engage in highly enantioselective conjugate additions with various arylboronic acids.

Original language	English
Pages (from-to)	14373-14375
Number of pages	3
Journal	Journal of the American Chemical Society
Volume	132
Issue number	41
DOIs	https://doi.org/10.1021/ja106809p
Publication status	Published - 20 Oct 2010

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title = "Enantioselective rhodium-catalyzed addition of arylboronic acids to alkenylheteroarenes",

abstract = "In the presence of a rhodium complex containing a newly developed chiral diene ligand, alkenes activated by a range of π-deficient or π-excessive heteroarenes engage in highly enantioselective conjugate additions with various arylboronic acids.",

author = "Graham Pattison and Guillaume Piraux and Lam, \{Hon Wai\}",

year = "2010",

month = oct,

day = "20",

doi = "10.1021/ja106809p",

language = "English",

volume = "132",

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journal = "Journal of the American Chemical Society",

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T1 - Enantioselective rhodium-catalyzed addition of arylboronic acids to alkenylheteroarenes

AU - Pattison, Graham

AU - Piraux, Guillaume

AU - Lam, Hon Wai

PY - 2010/10/20

Y1 - 2010/10/20

N2 - In the presence of a rhodium complex containing a newly developed chiral diene ligand, alkenes activated by a range of π-deficient or π-excessive heteroarenes engage in highly enantioselective conjugate additions with various arylboronic acids.

AB - In the presence of a rhodium complex containing a newly developed chiral diene ligand, alkenes activated by a range of π-deficient or π-excessive heteroarenes engage in highly enantioselective conjugate additions with various arylboronic acids.

UR - https://www.scopus.com/pages/publications/77958067774

U2 - 10.1021/ja106809p

DO - 10.1021/ja106809p

M3 - Article

C2 - 20879736

AN - SCOPUS:77958067774

SN - 0002-7863

VL - 132

SP - 14373

EP - 14375

JO - Journal of the American Chemical Society

JF - Journal of the American Chemical Society

IS - 41

ER -

Enantioselective rhodium-catalyzed addition of arylboronic acids to alkenylheteroarenes

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