The first asymmetric Suzuki cross-coupling reaction

Andrew N. Cammidge; Karen V. L. Crépy

doi:10.1039/B004513F

The first asymmetric Suzuki cross-coupling reaction

Andrew N. Cammidge, Karen V. L. Crépy

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

288 Citations (Scopus)

Abstract

The first asymmetric coupling reactions between aryl halides and aryl boronates (Suzuki coupling) are described to give binaphthalene derivatives in up to 85% ee.

Original language	English
Pages (from-to)	1723-1724
Number of pages	2
Journal	Chemical Communications
Issue number	18
DOIs	https://doi.org/10.1039/B004513F
Publication status	Published - 2000

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10.1039/B004513F

Cite this

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title = "The first asymmetric Suzuki cross-coupling reaction",

abstract = "The first asymmetric coupling reactions between aryl halides and aryl boronates (Suzuki coupling) are described to give binaphthalene derivatives in up to 85% ee.",

author = "Cammidge, {Andrew N.} and Cr{\'e}py, {Karen V. L.}",

year = "2000",

doi = "10.1039/B004513F",

language = "English",

pages = "1723--1724",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "18",

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AU - Cammidge, Andrew N.

AU - Crépy, Karen V. L.

PY - 2000

Y1 - 2000

N2 - The first asymmetric coupling reactions between aryl halides and aryl boronates (Suzuki coupling) are described to give binaphthalene derivatives in up to 85% ee.

AB - The first asymmetric coupling reactions between aryl halides and aryl boronates (Suzuki coupling) are described to give binaphthalene derivatives in up to 85% ee.

U2 - 10.1039/B004513F

DO - 10.1039/B004513F

M3 - Article

SP - 1723

EP - 1724

JO - Chemical Communications

JF - Chemical Communications

SN - 1359-7345

IS - 18

ER -