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Radical Esterification of Unactivated Alkenes Using Formate as Carbonyl Source
Ist Teil von
Journal of organic chemistry, 2022-04, Vol.87 (7), p.4918-4925
Ort / Verlag
United States: American Chemical Society
Erscheinungsjahr
2022
Quelle
MEDLINE
Beschreibungen/Notizen
In recent years, methyl formate has received considerable attention as an ideal and green C1 building block to synthesize carboxylic esters. However, examples of a one-step route to esters with one-carbon elongation using methyl formate as a source of methoxycarbonyl radical are still rare. Herein, we present peroxide-induced radical carbonylation of N-(2-methylallyl)benzamides with methyl formate as the precursor of methoxycarbonyl radical and RuCl3 as catalyst, affording a series of biologically valuable 4-[(methoxycarbonyl)methyl]-3,4-dihydroisoquinolinones with good tolerance and insensitivity to moisture in one pot under simple and mild conditions.