16691-59-1Relevant articles and documents
Highly Enantioselective Synthesis of Cyclic Aminals with a Cyclopentadiene-Based Chiral Carboxylic Acid
Sui, Yuebo,Cui, Peng,Liu, Sensheng,Zhou, Yanmei,Du, Peng,Zhou, Haifeng
supporting information, p. 215 - 218 (2018/01/26)
A highly enantioselective aminalization of 2-aminobenzenesulfonamides and aldehydes catalyzed by a novel cyclopentadiene-based chiral carboxylic acid has been realized. The cost-effective and readily synthesized cyclopentadiene-based chiral carboxylic aci
Thermal Rearrangements and Reactions of 5-Alkyl-1,2,3,4,5-pentakis(methoxycarbonyl)cyclopentadienes
Jefferson, Elizabeth A.,Warkentin, John
, p. 463 - 467 (2007/10/02)
Studies of the thermal reactions of five 5-alkyl-1,2,3,4,5-pentakis(methoxycarbonyl)cyclopentadienes in methanol solvent are described, where the alkyl groups are benzhydryl, methoxymethyl, 1-adamantyl, p-methoxybenzyl, and benzyl.The benzyl cyclopentadiene system undergoes thermal -sigmatropic rearrangement via methoxycarbonyl migrations while the other cyclopentadienes undergo C-alkyl bond heterolysis to ion-pair intermediates, which are scavenged by solvent.First-order rate constants for solvolysis of the methoxymethyl, 1-adamantyl, and p-methoxymethyl systems in methanol solvent were determined and that for the benzhydryl system was estimated from a single measurement of the half-life.