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Divergent Synthesis of Silacycles by Ligand-Controlled Rhodium-Catalyzed Annulation of (2-Hydrosilylaryl)acetylenes
被引:0
|作者:
Fuji, Kazuto
[2
]
Kawashima, Kyohei
[1
]
Mori, Toshifumi
[1
,2
]
Sekine, Kohei
[1
,2
]
Kuninobu, Yoichiro
[1
,2
]
机构:
[1] Kyushu Univ, Inst Mat Chem & Engn, 6-1 Kasugakoen, Kasuga Shi, Fukuoka 8168580, Japan
[2] Kyushu Univ, Interdisciplinary Grad Sch Engn Sci, Dept Interdisciplinary Engn Sci, Kasuga Shi, Fukuoka 8168580, Japan
关键词:
HYDRIDE-PROMOTED CYCLIZATION;
TRANS-HYDROSILYLATION;
ALKYNES;
BENZOSILOLES;
HETEROCYCLES;
DERIVATIVES;
SITE;
D O I:
10.1021/acs.orglett.4c04694
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
This study demonstrates the rhodium-catalyzed divergent synthesis of 5-, 5,6-, and 8-membered silacyclic compounds, such as benzosilole, silolosiline, and disilocine, from (2-hydrosilylaryl)acetylenes. To achieve high product selectivity, intra- and intermolecular reactions are controlled by tuning the mono- and bidentate phosphine ligands on the rhodium catalyst precursor. Deuterium labeling experiments and computational studies reveal that the annulation reaction proceeds via hydride transfer to the alkyne moiety.
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页码:1614 / 1619
页数:6
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