期刊
ORGANIC LETTERS
卷 -, 期 -, 页码 1447-1452出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.3c00178
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An efficient Pd-II- and Rh-III-controlled site-selective C-H bond alkynylation of imidazopyridines using (bromoethynyl)triisopropylsilane is described, providing access to a wide range of products alkynylated at the C3 and ortho positions. This methodology shows potential as a practical platform for late stage diversification and could aid in the development of more selective and complementary catalytic systems.
An efficient Pd-II- and Rh-III-controlled site-selective C-H bond alkynylation of imidazopyridines using (bromoethynyl)triisopropylsilane is disclosed. The divergent methodology allows straightforward access to a wide range of products alkynylated at the C3 and ortho positions. This strategy is suggestive of a practical platform that can be suitable for late stage diversification and may assist in the design of more selective and complementary catalytic systems.
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