Alkoxycarbonylation reactions involve the addition of a carbonyl group (C=O) and an alkoxy group (-OR) to a substrate. Palladium-catalyzed alkoxycarbonylation of β-lactam vinyl triflates is a versatile method for the synthesis of β-lactams bearing carbonyl functionality. The reaction may proceed through the insertion of carbon monoxide (CO) into the Pd-alkyl intermediate followed by trapping with an alcohol nucleophile.
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(6R,7S)-8-Oxo-7-(2-phenoxy-acetylamino)-1-aza-bicyclo[4.2.0]oct-2-ene-2,3-dicarboxylic acid 3-methyl ester 2-(4-nitro-benzyl) ester
4-ETHYLPHENYL 4-ETHYLBENZENECARBOXYLATE
Carbamic acid, acetylphenyl-, 1,1-dimethylethyl ester
ethyl 3,3-bis(4-(trifluoromethyl)phenyl)acrylate
ethyl 4-(2-chlorophenoxy)butanoate
2-Nonen-4-ynal, 3-phenyl-, (2Z)-
