4370-81-4Relevant articles and documents
Mechanistic investigation of the selective reduction of Meldrum's acids to β-hydroxy acids using SmI2 and H2O
Szostak, Michal,Lyons, Sarah E.,Spain, Malcolm,Procter, David J.
supporting information, p. 8391 - 8394 (2014/07/22)
The mechanism of a recently reported first mono-reduction of cyclic 1,3-diesters (Meldrum's acids) to β-hydroxy acids with SmI 2-H2O has been studied using a combination of reactivity, deuteration, kinetic isotope and radical clock e
Nickel-catalyzed highly selective hydrovinylation of α-ketals of vinylarenes
Zhang, Qi,Zhu, Shou-Fei,Qiao, Xiang-Chen,Wang, Li-Xin,Zhou, Qi-Lin
supporting information; experimental part, p. 1507 - 1510 (2009/07/30)
A nickel-catalyzed hydrovinylation of α-ketal derivatives of vinylarenes has been developed, providing a new method for preparing functional olefins with a quarternary carbon center in high yields and selectivities.
Note on the hydrolytic desulphuration of some heterocyclic thiones using silver nitrate
Geffken
, p. 363 - 365 (2007/10/10)
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