Catalytic Reactions of Terminal Alkynes Using Rhodium(I) Complexes Bearing 8-Quinolinolate Ligands

被引:20
作者
Kakiuchi, Fumitoshi [1 ]
Takano, Shotaro [1 ]
Kochi, Takuya [1 ]
机构
[1] Keio Univ, Fac Sci & Technol, Dept Chem, Kohoku Ku, 3-14-1 Hiyoshi, Yokohama, Kanagawa 2238522, Japan
关键词
8-quinolinolate ligands; terminal alkynes; hydroalkoxylation; hydroamination; hydrothiolation; anti-Markovnikov addition; alkyne/alkyne coupling; alkyne/alkene coupling; ANTI-MARKOVNIKOV ADDITION; SELECTIVE H/D EXCHANGE; TO-TAIL DIMERIZATION; INTERMOLECULAR HYDROAMINATION; SECONDARY-AMINES; METAL VINYLIDENES; ORGANOMETALLIC COMPLEXES; IRIDIUM(I) COMPLEXES; MOLECULAR-STRUCTURE; BIDENTATE LIGANDS;
D O I
10.1021/acscatal.8b01286
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
8-Quinolinolate is a monoanionic, hard, strongly 6-donating ligand that can form strong chelates with various metals. However, studies of the catalytic activities of soft transition metal complexes such as greater than second row, low-valent, late-transition metals having 8-quinolinolate ligands had not been well explored until recently. In recent years, several research groups including our own have studied and developed various reactions of terminal alkynes using rhodium(I) catalysts containing an 8-quinolinolate ligand. In this Perspective, we surveyed the transformations of terminal alkynes using 8-quinolinolato rhodium(I) catalyst such as additions of alcohols, amines, and thiols as well as polymerization, trimerization, dimerization, and alkyne/alkene [2 + 2] cycloaddition. Mechanistic studies based on theoretical calculations of hydroalkoxylation of alkynes and alkyne/alkene [2 + 2] cycloaddition reactions have also been described.
引用
收藏
页码:6127 / 6137
页数:21
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