1914-13-2Relevant articles and documents
Electrophilic Reactions of Carbonyl Compounds and their Derivatives. VI. Vinyl Ethers and Chlorinated Hydrocarbons in the Synthesis of Pyrylium Salts
Luk'yanov, S. M.
, p. 794 - 800 (2007/10/03)
Two- and three-component condensations of α-ethoxystyrene with carbonyl compounds and their derivatives serving as a source of heterocarbenium and hydroxyallyl cations are studied.The reactions result in formation of monocyclic pyrilium salts.
THERMAL YLIDE REARRANGEMENT AND BASE CATALYZED METHYLSULFONIO GROUP MIGRATION OF METHYLSULFONIUM 1-(2,6-DIPHENYL AND 2,3,5,6-TETRAPHENYL-4H-PYRAN-4-YL)-2-OXO-2-PHENYLETHYLIDES
Toda, Takashi,Tokida, Akihiko,Mukai, Toshio,Suzuki, Yoshizo
, p. 1535 - 1538 (2007/10/02)
Thermolyses of dimethylsulfonium 1-(2,6-diphenyl and 2,3,5,6-tetraphenyl-4H-pyran-4-yl)-2-oxo-2-phenylethylides (1 and 3) caused a novel ylide rearrangement to give dimethylsulfonium 1-benzoyl-6-oxo-2,6-diphenyl and 2,3,5,6-tetraphenyl-2,4-hexadienylides (6 and 7) respectively.The formations of oxy-thio-acetal derivatives (11 and 12) of 4-pyranylidene from 3 and its methylphenylsulfonium analogue (4) by base treatment are also reported.