Synthesis of a class of binaphthyl monophosphine ligands with a naphthofuran skeleton and their applications in Suzuki-Miyaura coupling reactions

Zihong Zhou; Hao Liang; Wang Xia; Huixuan Chen; Yaqi Zhang; Xuefeng He; Sifan Yu; Rihui Cao; Liqin Qiu

doi:10.1039/c8nj00412a

Synthesis of a class of binaphthyl monophosphine ligands with a naphthofuran skeleton and their applications in Suzuki-Miyaura coupling reactions

Zihong Zhou
, Hao Liang
, Wang Xia
, Huixuan Chen
, Yaqi Zhang
, Xuefeng He
, Sifan Yu
, Rihui Cao
, Liqin Qiu^*

^*Corresponding author for this work

Chinese Medicine - Teaching and Research Division

Research output: Contribution to journal › Journal article › peer-review

14 Citations (Scopus)

Abstract

A series of new monophosphine ligands containing a naphthofuran skeleton have been prepared, characterized and evaluated in palladium-catalyzed Suzuki-Miyaura coupling reactions. Using Pd₂(dba)₃-L6 as the catalyst the reactions were performed with high catalytic activity under mild reaction conditions and the desired coupling products were obtained in good to excellent yields. The new catalyst system also showed broad substrate adaptability and practicality for gram-scale production.

Original language	English
Pages (from-to)	5967-5971
Number of pages	5
Journal	New Journal of Chemistry
Volume	42
Issue number	8
Early online date	13 Mar 2018
DOIs	https://doi.org/10.1039/c8nj00412a
Publication status	Published - 21 Apr 2018

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title = "Synthesis of a class of binaphthyl monophosphine ligands with a naphthofuran skeleton and their applications in Suzuki-Miyaura coupling reactions",

abstract = "A series of new monophosphine ligands containing a naphthofuran skeleton have been prepared, characterized and evaluated in palladium-catalyzed Suzuki-Miyaura coupling reactions. Using Pd2(dba)3-L6 as the catalyst the reactions were performed with high catalytic activity under mild reaction conditions and the desired coupling products were obtained in good to excellent yields. The new catalyst system also showed broad substrate adaptability and practicality for gram-scale production.",

author = "Zihong Zhou and Hao Liang and Wang Xia and Huixuan Chen and Yaqi Zhang and Xuefeng He and Sifan Yu and Rihui Cao and Liqin Qiu",

note = "We would like to thank the National Natural Science Foundation of China (NSFC) (21272283), the Special Financial Fund of Innovative Development of Marine Economic Demonstration Project (GD2012-D01-001), and the Dayawan District Science and Technology Program (201202002) for financial support. Publisher Copyright: {\textcopyright} The Royal Society of Chemistry and the Centre National de la Recherche Scientifique 2018",

year = "2018",

month = apr,

day = "21",

doi = "10.1039/c8nj00412a",

language = "English",

volume = "42",

pages = "5967--5971",

journal = "New Journal of Chemistry",

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publisher = "Royal Society of Chemistry",

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TY - JOUR

T1 - Synthesis of a class of binaphthyl monophosphine ligands with a naphthofuran skeleton and their applications in Suzuki-Miyaura coupling reactions

AU - Zhou, Zihong

AU - Liang, Hao

AU - Xia, Wang

AU - Chen, Huixuan

AU - Zhang, Yaqi

AU - He, Xuefeng

AU - Yu, Sifan

AU - Cao, Rihui

AU - Qiu, Liqin

N1 - We would like to thank the National Natural Science Foundation of China (NSFC) (21272283), the Special Financial Fund of Innovative Development of Marine Economic Demonstration Project (GD2012-D01-001), and the Dayawan District Science and Technology Program (201202002) for financial support. Publisher Copyright: © The Royal Society of Chemistry and the Centre National de la Recherche Scientifique 2018

PY - 2018/4/21

Y1 - 2018/4/21

N2 - A series of new monophosphine ligands containing a naphthofuran skeleton have been prepared, characterized and evaluated in palladium-catalyzed Suzuki-Miyaura coupling reactions. Using Pd2(dba)3-L6 as the catalyst the reactions were performed with high catalytic activity under mild reaction conditions and the desired coupling products were obtained in good to excellent yields. The new catalyst system also showed broad substrate adaptability and practicality for gram-scale production.

AB - A series of new monophosphine ligands containing a naphthofuran skeleton have been prepared, characterized and evaluated in palladium-catalyzed Suzuki-Miyaura coupling reactions. Using Pd2(dba)3-L6 as the catalyst the reactions were performed with high catalytic activity under mild reaction conditions and the desired coupling products were obtained in good to excellent yields. The new catalyst system also showed broad substrate adaptability and practicality for gram-scale production.

UR - https://www.scopus.com/pages/publications/85045584887

U2 - 10.1039/c8nj00412a

DO - 10.1039/c8nj00412a

M3 - Journal article

AN - SCOPUS:85045584887

SN - 1144-0546

VL - 42

SP - 5967

EP - 5971

JO - New Journal of Chemistry

JF - New Journal of Chemistry

IS - 8

ER -

Synthesis of a class of binaphthyl monophosphine ligands with a naphthofuran skeleton and their applications in Suzuki-Miyaura coupling reactions

Abstract

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