154045-64-4Relevant academic research and scientific papers
New procedures for the selective synthesis of 2(2H)-pyranone derivatives and 3-aryl-4-iodoisocoumarins
Biagetti, Matteo,Bellina, Fabio,Carpita, Adriano,Stabile, Paolo,Rossi, Renzo
, p. 5023 - 5038 (2007/10/03)
5-Iodo-2(2H)-pyranone derivatives have been selectively synthesized by reaction of stereodefined methyl 2-en-4-ynoates with iodine in MeCN, CH2Cl2 or C6H6 at 20°C (Method C) or by treatment of these esters with
Regioselectivity in the Reductive Cleavage of Pyrogallol Derivatives: Reductive Electrophilic Substitution of Acetals of 2,3-Dimethoxyphenol
Azzena, Ugo,Melloni, Giovanni,Pisano, Luisa
, p. 261 - 266 (2007/10/02)
Acetals of 2,3-dimethoxyphenol were used as the starting materials for the transformation of 1,2,3-trioxygenated benzenes into various 1-oxygenated-2,3-dicarbon-substituted benzenes, via regioselective reductive electrophilic substitution of the 2-methoxy
Reductive Electrophilic Substitution of Pyrogallol Derivatives: Synthesis of 2,3-Disubstituted Phenols
Azzena, Ugo,Melloni, Giovanni,Pisano, Luisa
, p. 5635 - 5638 (2007/10/02)
1,2-Dimethoxy-3-methoxymethoxybenzene, 1, was used as the starting material for the transformation of a 1,2,3-trioxybenzene into various 1-oxy-2,3-dicarbobenzenes, via regioselective reductive electrophilic substitution of the 2-methoxy group followed by
