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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2019 Volume 29, Issue 1, Pages 19–21 (Mi mendc1407)

This article is cited in 1 paper

Communications

Unusual iodination of arylsulfonylallenes

S. V. Lozovskiya, A. V. Vasilyevab

a Institute of Chemistry, St. Petersburg State University, St. Petersburg, Russian Federation
b St. Petersburg State Forest Tecnical University, St. Petersburg, Russian Federation

Abstract: Arysulfonylallenes (ArSO2–CR1=C=CR2R3), depending on their structure, react with iodine to give two types of products, diiodo alkenes ArSO2–CHI–CI=CR2R3, when R1=H, or iodo dienes ArSO2–CR1=CI–C(Me)=CH2, when R1=Br, Ph and R2=R3=Me, in yields of 55–98%. The plausible reaction mechanisms have been proposed.

Language: English

DOI: 10.1016/j.mencom.2019.01.005



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