๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Control of carbenoid reactivity through neighboring group participation

โœ Scribed by Huw M.L. Davies; Julius J. Matasi; Craig Thornley


Book ID
103406387
Publisher
Elsevier Science
Year
1995
Tongue
French
Weight
195 KB
Volume
36
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Neighboring group participation in photo
โœ R. Staudenmayer; T.D. Roberts ๐Ÿ“‚ Article ๐Ÿ“… 1974 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 232 KB

Acetanilides should fragment and rearrange in ultraviolet light.2 However, if a suitable neighboring group is available in the ortho position other reactions may occur. For example, irradiation of R-cyanoacetanilide, I\_, in aqueous solvents provides not only the expected cleavage and rearrangement

Neighboring group participation in polar
โœ Samuel P. McManus; Randy A. Hames ๐Ÿ“‚ Article ๐Ÿ“… 1973 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 163 KB

Recent studies by ingly demonstrated that the benzylic cations (1) rather Fahey and Schneider' and by Yates and Rolston 3y4 have convincpolar bromination of styrene derivatives proceeds through open than cyclic bromonium ions (2). These findings are further supported by the more recent work of Wilki

Enhancement of neighboring group partici
โœ C.F. Wilcox Jr.; B. Brungardt ๐Ÿ“‚ Article ๐Ÿ“… 1984 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 291 KB

The solvolysis rates of a series of nitrile-substituted 2norbornyl tosylates are presented along with a semi-quantitative analysis of the rates.