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Radical reactions, domino processes substitution

An unprecedented domino radical cyclization/Smiles rearrangement process of 175 to give 3-(2-aryl-N-methylacetamido)indolin-2-ones 178 or 180 was reported by Gerard, Sapi, et al. [63] (Scheme 5.38). The reaction proceeds via a 5-exo-trig cyclization followed by radical substitution. The radical intermediate 177, formed via the radicals A and 176, could undergo either a normal termination of a radical to form product 178 in 11-66% yields or an additional amidyl radical cyclization, giving the product 180 in up to 40% yield depending on the reaction conditions. [Pg.167]


See other pages where Radical reactions, domino processes substitution is mentioned: [Pg.8]    [Pg.219]    [Pg.222]    [Pg.46]    [Pg.8]    [Pg.219]    [Pg.222]    [Pg.85]    [Pg.21]    [Pg.142]    [Pg.154]    [Pg.101]   
See also in sourсe #XX -- [ Pg.167 ]




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Domino processes

Domino radical reactions

Domino reactions

Process radical

Process substitution

Radical reaction substitution

Radicals 3-substituted

Substitution radical

Substitution reactions processes

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