A simple and versatile acetylene equivalent in Diels–Alder reactions
PR Kumar
Index: Kumar, Perumal Raja Journal of the Chemical Society, Chemical Communications, 1989 , p. 509 - 510
Full Text: HTML
Citation Number: 7
Abstract
Allyl phenyl sulphone and cinnamyl p-tolyl sulphone underwent cycloaddition with tetraphenylcyclopentadienone, indanocyclone, 1, 3-diphenylisobenzofuran, and tetraphenylcyclopentadiene to give the adducts with elimination of methyl phenyl sulphone and methyl p-tolyl sulphone respectively.
Related Articles:
[Cantrell, Gary L.; Filler, Robert Journal of Fluorine Chemistry, 1985 , vol. 29, p. 417 - 424]
[Fry, Albert J.; Sherman, Laura R.; Beaulieu, Alessandrina R.; Sherwin, Carol Journal of Organic Chemistry, 1990 , vol. 55, # 1 p. 389 - 391]
[Fry, Albert J.; Sherman, Laura R.; Beaulieu, Alessandrina R.; Sherwin, Carol Journal of Organic Chemistry, 1990 , vol. 55, # 1 p. 389 - 391]
[Tsutsui; Zeiss Journal of the American Chemical Society, 1959 , vol. 81, p. 6090]
[Blatter, Karsten; Schlueter, Arnulf-Dieter Chemische Berichte, 1989 , vol. 122, p. 1351 - 1356]