160661-43-8Relevant academic research and scientific papers
Stereoselective construction and synthetic applications of phenylthio substituted iodoolefins
Magriotis,Doyle,Kim
, p. 2541 - 2544 (1990)
(E)- and (Z)-Phenylthio substituted iodoolefins 1 and 2 have been synthesized stereoselectively via lower order stannylcuprate addition to and hydroalumination of appropriate alkyne precursors. Their utility in model studies on the synthesis of calichemic
An investigation of the behaviour of α,β-unsaturated sulfoxides in the presence of trimethylsilyl iodide
Aversa, Maria C.,Barattucci, Anna,Bonaccorsi, Paola,Giannetto, Placido
, p. 10145 - 10150 (2007/10/03)
A mild, efficient and seemingly general method for converting α,β-unsaturated sulfoxides into carbonyl compounds by means of trimethylsilyl iodide (TMSI) is described. Experiments on different substrates and trimethylsilyl halides lead to the conclusion that the oxidation state of the sulfur atom, on one hand, and halogen kind in TMSX on the other, assume a determining role in the progression of the reaction. The ease of experimental procedure, the possibility of 1H NMR monitoring, and good yields of final products constitute advantages of the TMSI-promoted conversion of α,β-unsaturated sulfoxides into carbonyl compounds.
NUCLEOPHILIC REACTION AT A VINYL CENTER. XXII. SYNTHESIS AND NUCLEOPHILIC VINYLIC SUBSTITUTION IN E-β-FLUOROVINYL ARYL SULFONES
Shainyan, B. A.,Mirskova, A. N.
, p. 61 - 66 (2007/10/02)
The reaction of potassium fluoride with E-β-bromovinyl aryl sulfones in the presence of 18-crown-6-ether leads to a mixture of the sulfones XC6H4SO2CH2CHF2 and E-XC6H4SO2CH=CHF, the ratio of which decreases in the order X=CH3, H, Cl, NO2.The kinetics of n
