Base-Catalyzed Intramolecular Hydroamination of Conjugated Enynes
Wen Zhang, Jenny B. Werness, Weiping Tang
Abstract
Wen Zhang, Jenny B. Werness, Weiping Tang
Abstract
A de novo intramolecular hydroamination of conjugated enynes was developed using commercially available n-BuLi as a precatalyst. This hydroamination reaction successfully afforded allenyl-substituted pyrrolidines with up to 95% yield. One of the resulting allenyl pyrrolidines was converted to the natural products irniine and irnidine in three steps.
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A de novo intramolecular hydroamination of conjugated enynes was developed using commercially available n-BuLi as a precatalyst. This hydroamination reaction successfully afforded allenyl-substituted pyrrolidines with up to 95% yield. One of the resulting allenyl pyrrolidines was converted to the natural products irniine and irnidine in three steps.
Key concepts: Hydroamination, Intramolecular force, Chemistry, Conjugated system, Catalysis, Yield (engineering), Combinatorial chemistry, Organic chemistry