4.8 Article

Selective [3+2] Cycloaddition of Cyclopropenone Derivatives and Elemental Chalcogens

Journal

ORGANIC LETTERS
Volume 22, Issue 14, Pages 5555-5560

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.0c01914

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Funding

  1. National Natural Science Foundation of China [21901187]

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A highly efficient method is disclosed for the synthesis of 1,2-dichalcogen heterocycles via [3 + 2] cycloaddition of cyclopropenone derivatives and elemental chalcogens. Different from other cyclopropenone derivatives, cyclopropenselenones undergo unprecedented rearrangement with elemental sulfur. The features of this protocol include mild reaction conditions, high efficiency, excellent atom economy, gram-scale ability, and good regioselectivity.

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