Rhodium-Catalyzed Ring Opening of Benzocyclobutenols with Site-Selectivity Complementary to Thermal Ring Opening

Rhodium-Catalyzed Ring Opening of Benzocyclobutenols with Site-Selectivity Complementary to Thermal Ring Opening
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DOI:
10.1021/ja309013a
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发表时间:
2012-10-24
影响因子:
15
通讯作者:
Murakami, Masahiro
Murakami, Masahiro
中科院分区:
化学1区
文献类型:
--
作者:
Ishida, Naoki;Sawano, Shota;Murakami, Masahiro

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铑催化剂诱导苯并环丁烯醇开环,并选择性裂解与羟基相邻的C(sp(2))-C(sp(3))键。其位置选择性与热开环反应形成鲜明对比。铑催化的开环导致了一个新的炔插入反应的发展,构建一个二氢萘框架。
A rhodium catalyst induced ring opening of benzocyclobutenols with selective cleavage of the C(sp(2))-C(sp(3)) bond adjacent to the hydroxyl group. The site-selectivity markedly contrasted with that of their thermal ring-opening reaction. The rhodium-catalyzed ring opening led to the development of a new alkyne insertion reaction constructing a dihydronaphthalene framework.