57465-41-5Relevant academic research and scientific papers
Efficient synthesis of 3-arylbutadiene sulfones using the Heck–Matsuda reaction
Asachenko, Andrey F.,Bogachev, Vasilii N.,Minaeva, Lidiya I.,Nechaev, Mikhail S.,Rzhevskiy, Sergey A.,Sterligov, Grigorii K.,Topchiy, Maxim A.
, p. 548 - 549 (2021/08/24)
An efficient and practical method for a scalable synthesis of 3-arylbutadiene sulfones deals with the ligand-free Heck–Matsuda reaction of sulfolene with aryldiazonium tetrafluoroborates followed by triethylamine-promoted double bond shift.
Stoichiometric release of SO2 from adducts: Application to the direct synthesis of protected dienes
Martial, Ludovic,Bischoff, Laurent
supporting information, p. 1225 - 1229 (2015/06/02)
Abstract The in situ, stoichiometric release of SO2 was studied from DABSO (DABCO adduct with SO2) and DMAP adduct. When involved in cheletropic additions, free SO2 released by this technique proved much more reactive than its adducts. Some examples of applications towards the direct synthesis of protected dienes from allylic alcohols are given.
Pharmaceutical compositions as inhibitors of dipeptidyl peptidase-IV (DPP-IV)
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Page/Page column 26, (2010/11/26)
The present invention relates to compounds, which inhibit dipeptidyl peptidase IV (DPP-IV) and are useful for the prevention or treatment of diabetes, especially type II, as well as hyperglycemia, metabolic syndrome, hyperinsulinemia, obesity, atheroscler
Palladium-Catalyzed Cross-Coupling Reactions of 3-Tributylstannylsulfolene
Bew, Sean P.,Sweeney
, p. 1273 - 1274 (2007/10/03)
3-Tributylstannylsulfolene (1) undergoes palladium-catalyzed cross-coupling reactions with aryl and vinyl halides, cyclohex-1-enyl triflates and acyl chlorides in moderate to excellent yield, thereby allowing rapid entry to a diverse range of 3-substitute
