Homocoupling of alkyl-, alkenyl-, and arylboronic acids

J. R. Falck; Suchismita Mohapatra; Muralidhar Bondlela; Sylesh K. Venkataraman

doi:10.1016/S0040-4039(02)01897-X

Homocoupling of alkyl-, alkenyl-, and arylboronic acids

J. R. Falck, Suchismita Mohapatra, Muralidhar Bondlela, Sylesh K. Venkataraman

Biochemistry

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

54 Scopus citations

Abstract

Alkyl-, alkenyl-, and arylboronic acids undergo Ag₂O/CrCl₂ mediated homocoupling in moderate to good yields under mild conditions. The general utility of this methodology is illustrated by an intramolecular annulation between sp and sp³ centers.

Original language	English (US)
Pages (from-to)	8149-8151
Number of pages	3
Journal	Tetrahedron Letters
Volume	43
Issue number	45
DOIs	https://doi.org/10.1016/S0040-4039(02)01897-X
State	Published - Nov 4 2002

Keywords

Annulation
Boron
Chromium
Coupling reactions
Dimerisation

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(02)01897-X

Cite this

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title = "Homocoupling of alkyl-, alkenyl-, and arylboronic acids",

abstract = "Alkyl-, alkenyl-, and arylboronic acids undergo Ag2O/CrCl2 mediated homocoupling in moderate to good yields under mild conditions. The general utility of this methodology is illustrated by an intramolecular annulation between sp and sp3 centers.",

keywords = "Annulation, Boron, Chromium, Coupling reactions, Dimerisation",

author = "Falck, {J. R.} and Suchismita Mohapatra and Muralidhar Bondlela and Venkataraman, {Sylesh K.}",

note = "Funding Information: Supported financially by the USPHS NIH (GM31278, DK38226), the Robert A. Welch Foundation, and an unrestricted grant from Taisho Pharmaceutical Co., Ltd.",

year = "2002",

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doi = "10.1016/S0040-4039(02)01897-X",

language = "English (US)",

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pages = "8149--8151",

journal = "Tetrahedron Letters",

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TY - JOUR

T1 - Homocoupling of alkyl-, alkenyl-, and arylboronic acids

AU - Falck, J. R.

AU - Mohapatra, Suchismita

AU - Bondlela, Muralidhar

AU - Venkataraman, Sylesh K.

N1 - Funding Information: Supported financially by the USPHS NIH (GM31278, DK38226), the Robert A. Welch Foundation, and an unrestricted grant from Taisho Pharmaceutical Co., Ltd.

PY - 2002/11/4

Y1 - 2002/11/4

N2 - Alkyl-, alkenyl-, and arylboronic acids undergo Ag2O/CrCl2 mediated homocoupling in moderate to good yields under mild conditions. The general utility of this methodology is illustrated by an intramolecular annulation between sp and sp3 centers.

AB - Alkyl-, alkenyl-, and arylboronic acids undergo Ag2O/CrCl2 mediated homocoupling in moderate to good yields under mild conditions. The general utility of this methodology is illustrated by an intramolecular annulation between sp and sp3 centers.

KW - Annulation

KW - Boron

KW - Chromium

KW - Coupling reactions

KW - Dimerisation

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U2 - 10.1016/S0040-4039(02)01897-X

DO - 10.1016/S0040-4039(02)01897-X

M3 - Article

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VL - 43

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EP - 8151

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 45

ER -

Homocoupling of alkyl-, alkenyl-, and arylboronic acids

Abstract

Keywords

ASJC Scopus subject areas

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