This research demonstrates effective regioselective control in cycloaddition reactions, highlighting potential applications in organic synthesis.
A copper-catalyzed diastereoselective cross [3+3] dipolar cycloaddition of ethynyl methylene cyclic carbamates with N,N'-cyclic azomethine imines has been realized. The presence of an extended C═C bond in N,N'-cyclic azomethine imines distinctively changes the reaction pathway, enabling the precise regioselective control of ethynyl methylene cyclic carbamates serving as C1,C3-dipoles rather than sterically favorable C1,N-ones, thus delivering a range of N-(7-ethynyl-3-oxo-7-phenyl-8-((E)-styryl)-2,3,7,8-tetrahydro-1H-pyrazolo[1,2-a]pyridazin-6-yl)benzenesulfonamides in up to 93% yields.
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Li et al. (2026) studied this question.
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