Versatile palladium(II)-catalyzed Suzuki-Miyaura coupling in ethanol with a novel, stabilizing ligand

Jin-Jiao Ning; Jian-Feng Wang; Zhi-Gang Ren; David James Young; Jian-Ping Lang

doi:10.1016/j.tet.2015.04.052

Versatile palladium(II)-catalyzed Suzuki-Miyaura coupling in ethanol with a novel, stabilizing ligand

Jin-Jiao Ning, Jian-Feng Wang, Zhi-Gang Ren, David James Young, Jian-Ping Lang

Malaysia Sch of Science

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

14 Citations (Scopus)

Abstract

Suzuki-Miyaura coupling reactions of arylboronic acids with aryl bromides were mediated by PdCl2 and bdppmapy (N,N-bis-(diphenylphosphanylmethyl)-2-aminopyridine) that both stabilizes and solubilizes the catalyst in predominantly ethanol as a solvent. Excellent yields for a wide variety of substrates were obtained under relatively mild conditions in this green solvent.

Original language	English
Pages (from-to)	4000 - 4006
Number of pages	7
Journal	Tetrahedron
Volume	71
Issue number	23
DOIs	https://doi.org/10.1016/j.tet.2015.04.052
Publication status	Published - 2015

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10.1016/j.tet.2015.04.052

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title = "Versatile palladium(II)-catalyzed Suzuki-Miyaura coupling in ethanol with a novel, stabilizing ligand",

abstract = "Suzuki-Miyaura coupling reactions of arylboronic acids with aryl bromides were mediated by PdCl2 and bdppmapy (N,N-bis-(diphenylphosphanylmethyl)-2-aminopyridine) that both stabilizes and solubilizes the catalyst in predominantly ethanol as a solvent. Excellent yields for a wide variety of substrates were obtained under relatively mild conditions in this green solvent.",

author = "Jin-Jiao Ning and Jian-Feng Wang and Zhi-Gang Ren and Young, {David James} and Jian-Ping Lang",

year = "2015",

doi = "10.1016/j.tet.2015.04.052",

language = "English",

volume = "71",

pages = "4000 -- 4006",

journal = "Tetrahedron",

issn = "0040-4020",

publisher = "Elsevier",

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TY - JOUR

T1 - Versatile palladium(II)-catalyzed Suzuki-Miyaura coupling in ethanol with a novel, stabilizing ligand

AU - Ning, Jin-Jiao

AU - Wang, Jian-Feng

AU - Ren, Zhi-Gang

AU - Young, David James

AU - Lang, Jian-Ping

PY - 2015

Y1 - 2015

N2 - Suzuki-Miyaura coupling reactions of arylboronic acids with aryl bromides were mediated by PdCl2 and bdppmapy (N,N-bis-(diphenylphosphanylmethyl)-2-aminopyridine) that both stabilizes and solubilizes the catalyst in predominantly ethanol as a solvent. Excellent yields for a wide variety of substrates were obtained under relatively mild conditions in this green solvent.

AB - Suzuki-Miyaura coupling reactions of arylboronic acids with aryl bromides were mediated by PdCl2 and bdppmapy (N,N-bis-(diphenylphosphanylmethyl)-2-aminopyridine) that both stabilizes and solubilizes the catalyst in predominantly ethanol as a solvent. Excellent yields for a wide variety of substrates were obtained under relatively mild conditions in this green solvent.

UR - http://www.sciencedirect.com/science/article/pii/S0040402015005517

U2 - 10.1016/j.tet.2015.04.052

DO - 10.1016/j.tet.2015.04.052

M3 - Article

SN - 0040-4020

VL - 71

SP - 4000

EP - 4006

JO - Tetrahedron

JF - Tetrahedron

IS - 23

ER -

Versatile palladium(II)-catalyzed Suzuki-Miyaura coupling in ethanol with a novel, stabilizing ligand

Abstract

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