Suzuki-Miyaura cross-coupling of lithium n-alkylborates

Gang Zou; J R Falck

doi:10.1016/S0040-4039(01)01128-5

Suzuki-Miyaura cross-coupling of lithium n-alkylborates

Gang Zou, J R Falck

Biochemistry

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

51 Scopus citations

Abstract

The palladium-catalyzed cross-coupling of lithium n-alkylborates, generated in situ via addition of sec-butyl lithium to boronate esters, proceeds in moderate to good yields with a wide variety of electrophiles.

Original language	English (US)
Pages (from-to)	5817-5819
Number of pages	3
Journal	Tetrahedron Letters
Volume	42
Issue number	34
DOIs	https://doi.org/10.1016/S0040-4039(01)01128-5
State	Published - Aug 20 2001

Keywords

Alkylation
Boron
Coupling reactions
Palladium
Suzuki

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(01)01128-5

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title = "Suzuki-Miyaura cross-coupling of lithium n-alkylborates",

abstract = "The palladium-catalyzed cross-coupling of lithium n-alkylborates, generated in situ via addition of sec-butyl lithium to boronate esters, proceeds in moderate to good yields with a wide variety of electrophiles.",

keywords = "Alkylation, Boron, Coupling reactions, Palladium, Suzuki",

author = "Gang Zou and Falck, {J R}",

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

year = "2001",

month = aug,

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doi = "10.1016/S0040-4039(01)01128-5",

language = "English (US)",

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pages = "5817--5819",

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TY - JOUR

T1 - Suzuki-Miyaura cross-coupling of lithium n-alkylborates

AU - Zou, Gang

AU - Falck, J R

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

PY - 2001/8/20

Y1 - 2001/8/20

N2 - The palladium-catalyzed cross-coupling of lithium n-alkylborates, generated in situ via addition of sec-butyl lithium to boronate esters, proceeds in moderate to good yields with a wide variety of electrophiles.

AB - The palladium-catalyzed cross-coupling of lithium n-alkylborates, generated in situ via addition of sec-butyl lithium to boronate esters, proceeds in moderate to good yields with a wide variety of electrophiles.

KW - Alkylation

KW - Boron

KW - Coupling reactions

KW - Palladium

KW - Suzuki

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U2 - 10.1016/S0040-4039(01)01128-5

DO - 10.1016/S0040-4039(01)01128-5

M3 - Article

AN - SCOPUS:0035920614

SN - 0040-4039

VL - 42

SP - 5817

EP - 5819

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 34

ER -

Suzuki-Miyaura cross-coupling of lithium n-alkylborates

Abstract

Keywords

ASJC Scopus subject areas

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