Palladium-catalyzed Suzuki-Miyaura cross-couplings of aryl tosylates with potassium aryltrifluoroborates

Liang Zhang; Tianhao Meng; Jie Wu

doi:10.1021/jo7019064

Palladium-catalyzed Suzuki-Miyaura cross-couplings of aryl tosylates with potassium aryltrifluoroborates

Liang Zhang, Tianhao Meng, Jie Wu

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

102 Scopus citations

Abstract

(Chemical Equation Presented) Pd-catalyzed Suzuki-Miyaura cross-coupling reaction of aryl tosylates with potassium aryl trifluoroborate in the presence of bulky and electron-rich phosphine ligand is described. In addition, a useful chemoselective coupling of an aryl chloride in the presence of a tosyloxy group was demonstrated.

Original language	English
Pages (from-to)	9346-9349
Number of pages	4
Journal	Journal of Organic Chemistry
Volume	72
Issue number	24
DOIs	https://doi.org/10.1021/jo7019064
State	Published - 23 Nov 2007
Externally published	Yes

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@article{6639daee68174993af7a4a6676fe7178,

title = "Palladium-catalyzed Suzuki-Miyaura cross-couplings of aryl tosylates with potassium aryltrifluoroborates",

abstract = "(Chemical Equation Presented) Pd-catalyzed Suzuki-Miyaura cross-coupling reaction of aryl tosylates with potassium aryl trifluoroborate in the presence of bulky and electron-rich phosphine ligand is described. In addition, a useful chemoselective coupling of an aryl chloride in the presence of a tosyloxy group was demonstrated.",

author = "Liang Zhang and Tianhao Meng and Jie Wu",

year = "2007",

month = nov,

day = "23",

doi = "10.1021/jo7019064",

language = "英语",

volume = "72",

pages = "9346--9349",

journal = "Journal of Organic Chemistry",

issn = "0022-3263",

publisher = "American Chemical Society",

number = "24",

}

TY - JOUR

T1 - Palladium-catalyzed Suzuki-Miyaura cross-couplings of aryl tosylates with potassium aryltrifluoroborates

AU - Zhang, Liang

AU - Meng, Tianhao

AU - Wu, Jie

PY - 2007/11/23

Y1 - 2007/11/23

N2 - (Chemical Equation Presented) Pd-catalyzed Suzuki-Miyaura cross-coupling reaction of aryl tosylates with potassium aryl trifluoroborate in the presence of bulky and electron-rich phosphine ligand is described. In addition, a useful chemoselective coupling of an aryl chloride in the presence of a tosyloxy group was demonstrated.

AB - (Chemical Equation Presented) Pd-catalyzed Suzuki-Miyaura cross-coupling reaction of aryl tosylates with potassium aryl trifluoroborate in the presence of bulky and electron-rich phosphine ligand is described. In addition, a useful chemoselective coupling of an aryl chloride in the presence of a tosyloxy group was demonstrated.

UR - https://www.scopus.com/pages/publications/36649030584

U2 - 10.1021/jo7019064

DO - 10.1021/jo7019064

M3 - 文章

AN - SCOPUS:36649030584

SN - 0022-3263

VL - 72

SP - 9346

EP - 9349

JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

IS - 24

ER -

Palladium-catalyzed Suzuki-Miyaura cross-couplings of aryl tosylates with potassium aryltrifluoroborates

Abstract

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