The Journal of Organic Chemistry

Amozonolysis of cycloolefins

MI Fremery, EK Fields

Index: Fremery,M.I.; Fields,E.K. Journal of Organic Chemistry, 1964 , vol. 29, p. 2240 - 2243

Full Text: HTML

Citation Number: 16

Abstract

Discussion Ammonia proved to be relatively stable towards ozone2 in presence of the more reactive olefins. At-30" the degree of dissociation of anhydrous liquid ammonia was high enough to yield sufficient H+ and XHz-to add to the zwitterion (I) in the same manner as do the more common protonic solvents.

Related Articles:

Ruthenium-catalyzed N-alkylation of amines and sulfonamides using borrowing hydrogen methodology

[Hamid, M. Haniti S. A.; Allen, C. Liana; Lamb, Gareth W.; Maxwell, Aoife C.; Maytum, Hannah C.; et al. Journal of the American Chemical Society, 2009 , vol. 131, p. 1766 - 1774]

More Articles...