Access to Complex Scaffolds Through [2 + 2] Cycloadditions of Strained Cyclic Allenes.

J Am Chem Soc

Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095, United States.

Published: June 2024

We report the strain-induced [2 + 2] cycloadditions of cyclic allenes for the assembly of highly substituted cyclobutanes. By judicious choice of trapping agent, complex scaffolds bearing heteroatoms, fused rings, contiguous stereocenters, spirocycles, and quaternary centers are ultimately accessible. Moreover, we show that the resulting cycloadducts can undergo thermal isomerization. This study provides an alternative strategy to photochemical [2 + 2] cycloadditions for accessing highly functionalized cyclobutanes, while validating the use of underexplored strained intermediates for the assembly of complex architectures.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11459239PMC
http://dx.doi.org/10.1021/jacs.4c03369DOI Listing

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