Convenient Formation of Triarylphosphines by Nickel‐Catalyzed C–P Cross‐Coupling with Aryl Chlorides | Zendy

Sun Meng | Zendy; Zang YuShi | Zendy; Hou LeKai | Zendy; Chen XiangXiang | Zendy; Sun Wei | Zendy; Yang ShangDong | Zendy

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Convenient Formation of Triarylphosphines by Nickel‐Catalyzed C–P Cross‐Coupling with Aryl Chlorides

Author(s) -

Sun Meng,

Zang YuShi,

Hou LeKai,

Chen XiangXiang,

Sun Wei,

Yang ShangDong

Publication year - 2014

Publication title -

european journal of organic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.825

H-Index - 155

eISSN - 1099-0690

pISSN - 1434-193X

DOI - 10.1002/ejoc.201402660

Subject(s) - chemistry , phosphine , aryl , nickel , catalysis , bond cleavage , combinatorial chemistry , cleavage (geology) , functional group , coupling reaction , medicinal chemistry , organic chemistry , stereochemistry , alkyl , geotechnical engineering , fracture (geology) , engineering , polymer

A convenient strategy has been developed for the preparation of various phosphine ligands in good to excellent yields through a nickel‐catalyzed C–P bond‐forming step. This reaction proceeded smoothly and tolerated a variety of functional groups to provide a new method for the synthesis of important phosphine ligands through the direct cleavage of a C–Cl bond.

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