𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Catalysis of the enolization of acetone by mono- and dicarboxylate bases. The role of hydrogen bonding

✍ Scribed by Venimadhavan, S.; Shelly, Kevin P.; Stewart, Ross

Book ID
126231892
Publisher
American Chemical Society
Year
1989
Tongue
English
Weight
445 KB
Volume
54
Category
Article
ISSN
0022-3263

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Sequential mono-N-arylation of piperazin
Sequential mono-N-arylation of piperazine nitrogens. Part 2: The role of hydrogen bonding
✍ Jeffrey Eckert; Tze-Ming Chan; Rebecca M. Osterman; Joseph B. Lambert; Dinesh Ga πŸ“‚ Article πŸ“… 1999 πŸ› Elsevier Science 🌐 French βš– 259 KB

A mechanistic study of the simple sequential N-arylation of piperazine suggests that in an electron-withdrawing group (EWG) containing N-arylated piperazines, hydrogen bonding of the secondary amine hydrogen is important for its non-metal catalyzed conversion to N,N'-diaryl piperazines. A combinatio

1H n.m.r. study of the self-association
1H n.m.r. study of the self-association of acetone phenylhydrazone by hydrogen bonding
✍ C. I. Stassinopoulou; J. Petrou πŸ“‚ Article πŸ“… 1977 πŸ› John Wiley and Sons 🌐 English βš– 271 KB

## Abstract Proton magnetic resonance dilution studies of acetone phenylhydrazone were carried out in __n__‐heptane, carbon disulphide and hexachlorobutadiene solutions. Equilibrium constants and enthalpy values for the predominant self‐associated species are reported. Linear trimeric aggregates pr