128015-91-8Relevant articles and documents
Pd-catalyzed decarbonylative olefination of aryl esters: Towards a waste-free Heck reaction
Goossen, Lukas J.,Paetzold
, p. 1237 - 1241 (2007/10/03)
Easy and clean: A palladium (0)-catalyzed decarbonylative Heck olefination of activated esters of aryl, heteroaryl, and vinyl carboxylic acids opens up an opportunity for a novel waste-free Heck olefination process (see scheme).
ON THE NATURE OF RESONANCE INTERACTIONS IN SUBSTITUTED BENZENES. II. 13C NMR INVESTIGATIONS ON ARYL 4-X-BENZOATES
Dell'Erba, Carlo,Sancassan, Fernando,Leandri, Giuseppe,Novi, Marino,Petrillo, Giovanni,et al.
, p. 643 - 648 (2007/10/02)
The response of the carbonyl-carbon chemical shift to the substituent effect in aryl 4-X-benzoates 3-6 has been studied in CDCl3.The comparison with relevant data for methyl benzoates 1 and acetophenones 2 shows, along the 3-to-6 sequence, a gradual shift