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Cyclization of 5-alkynones with chromium alkylidene equivalents generated in situ from gem-dichromiomethanes. | LitMetric

Cyclization of 5-alkynones with chromium alkylidene equivalents generated in situ from gem-dichromiomethanes.

Chem Commun (Camb)

Division of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University, 3-1-1 Tsushimanaka, Kita-ku, Okayama 700-8530, Japan.

Published: August 2020

A rare example of cyclization with 5-alkynones, which possess non-polar alkynyl and less electrophilic polar keto carbonyl groups, was demonstrated. The key to promoting carbene/alkyne metathesis followed by alkylidenation with pendant C[double bond, length as m-dash]O double bonds was the Schrock-type nucleophilic reactivity of the generated chromium carbene equivalents from readily available diiodomethanes and CrCl by simple heating.

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Source
http://dx.doi.org/10.1039/d0cc03986aDOI Listing

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