Intramolecular cycloaddition reactions of N-sulfonyl nitrile imides bearing alkenyl groups.

…, Y Hayashi, Y Nagano, K Teramura

Index: Shimizu, Tomio; Hayashi, Yoshiyuki; Nagano, Yoshio; Teramura, Kazuhiro Bulletin of the Chemical Society of Japan, 1980 , vol. 53, # 2 p. 429 - 434

Full Text: HTML

Citation Number: 20

Abstract

The reaction of the p-tolyl (or phenyl) sulfonylhydrazones of some 2-(alkenyloxy) benzaldehydes with lead tetraacetate leads, via the nitrile imide intermediates, Ar–\ overset+ C= N–\ overset− N–SO 2–C 6 H 4–Xp, to intramolecular 1, 3-dipolar cycloadducts and 1- acetyl-2-aroyl-1-p-tolyl (or phenyl) sulfonyl hydrazines in 20–65% and 7–70% yields respectively, while the intermolecular reactions of the benzaldehyde p- ...

Related Articles:

Facile and Selective Deallylations of Esters under 'Aqueous' Free-Radical Conditions

[Perchyonok, V. Tamara; Ryan, Sarah J.; Langford, Steven J.; Hearn, Milton T.; Tuck, Kellie L. Synlett, 2008 , # 8 p. 1233 - 1235]

An efficient chemoselective etherification of phenols in polyfunctional aromatic compounds

[Pandey, Jyoti; Mishra, Mridul; Bisht, Surendra Singh; Sharma, Anindra; Tripathi, Rama P. Tetrahedron Letters, 2008 , vol. 49, # 4 p. 695 - 698]

More Articles...