๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

A theoretical study of the conformational behaviour of the S-methyl ester of dithiocarbazic acid

โœ Scribed by A. Amore-Bonapasta; C. Battistoni; A. Lapiccirella; E. Paparazzo

Publisher
Elsevier Science
Year
1982
Tongue
English
Weight
384 KB
Volume
90
Category
Article
ISSN
0022-2860

No coin nor oath required. For personal study only.

๐Ÿ“œ SIMILAR VOLUMES

Theoretical investigation of the conform
Theoretical investigation of the conformational behaviour of N-phenylbenzohydroxamic acid in solution
โœ Ilaria Ciofini ๐Ÿ“‚ Article ๐Ÿ“… 2004 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 202 KB

Using ab initio theoretical approaches, we investigated the relative stability of two of the possible isomers of N-phenylbenzohydroxamic acid, PhCONOHPh. In particular, within the framework of density functional theory (DFT), we studied the cis and trans conformational isomers of PhCONOHPh, both in

Theoretical studies on the acid hydrolys
Theoretical studies on the acid hydrolysis of methyl carbamate
โœ Ikchoon Lee; Chang Kon Kim; Byung Choon Lee ๐Ÿ“‚ Article ๐Ÿ“… 1987 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 499 KB

The mechanism of the A2 acid hydrolysis of methyl carbamate was investigated using MNDO method. The reaction was found to proceed in two steps: (1) the rate-determining nucleophilic attack of water on the carbonyl carbon of the N-protonated tautomer involving the tetrahedral TS; and (2) the fast sub