Selective oxidations by sulfur trioxide

V Mark, L Zengierski, VA Pattison…

Index: Mark,V. et al. Journal of the American Chemical Society, 1971 , vol. 93, # 14 p. 3538 - 3540

Full Text: HTML

Citation Number: 2

Abstract

Similarly, 2, 3, 4, 5, 6-pentabromotoluene yielded quantitatively pentabromobenzaldehyde, mp 281-283'. Both aldehydes were completely free of the corresponding acids, probably as a result of steric crowding in E, which prevents the removal of the third hydrogen from the benzylic carbon. The aldehyde-forming reaction seems to be characteristic of polyhalotoluenes and meta-substituted benzenes (m-xylene and mesitylene), since ...

Related Articles:

Synthesis and chemical behavior of perchlorophenylacetylene

[Ballester, Manuel; Castaner, Juan; Riera, Juan; Tabernero, Ignacio Journal of Organic Chemistry, 1986 , vol. 51, # 9 p. 1413 - 1419]

Synthesis and chemical behavior of perchlorophenylacetylene

[Ballester, Manuel; Castaner, Juan; Riera, Juan; Tabernero, Ignacio Journal of Organic Chemistry, 1986 , vol. 51, # 9 p. 1413 - 1419]

Synthesis and chemical behavior of perchlorophenylacetylene

[Ballester, Manuel; Castaner, Juan; Riera, Juan; Tabernero, Ignacio Journal of Organic Chemistry, 1986 , vol. 51, # 9 p. 1413 - 1419]

Synthesis and chemical behavior of perchlorophenylacetylene

[Ballester, Manuel; Castaner, Juan; Riera, Juan; Tabernero, Ignacio Journal of Organic Chemistry, 1986 , vol. 51, # 9 p. 1413 - 1419]

Stereoselective nucleophilic additions to the carbon-nitrogen double bond. 3. Chiral acyliminium ions

[Polniaszek, Richard P.; Belmont, Stephen E.; Alvarez, Ramon Journal of Organic Chemistry, 1990 , vol. 55, # 1 p. 215 - 223]

More Articles...