77189-50-5Relevant academic research and scientific papers
REACTION OF NEW CYCLIC SULFUR YLIDES, 8-THIAAZULENES WITH ELECTROPHILES
Hori, Mikio,Kataoka, Tadashi,Shimizu, Hiroshi,Okitsu, Mitsuhito
, p. 721 - 724 (2007/10/02)
The reactions of 8-alkyl-1,3-diphenyldibenzo-8-thiaazulenes with acetylenic electrophiles yielded the considerably stable ylides.The ylides newly formed were not rearranged on refluxing in THF for 1 h, but caused the intramolecular 1,4-rearrangement
NEW CYCLIC SULFUR YLIDES, 8-THIAAZULENES. SYNTHESIS AND THERMAL REARRANGEMENTS OF 8-ALKYL-1,3-DIPHENYLDIBENZO-8-THIAAZULENES
Hori, Mikio,Kataoka, Tadashi,Shimizu, Hiroshi,Okitsu, Mitsuhito
, p. 4287 - 4290 (2007/10/02)
A new cyclic sulfur ylide, 1,3-diphenyl-8-methyldibenzo-8-thiaazulene was synthesized. 8-Alkyl-1,3-diphenyldibenzo-8-thiaazulenes were thermally rearranged to give 1,2-rearranged products and 1,4-rearranged products.
