There is good evidence that intramolecular general base catalysis is much less efficient than intramolecular nucleophilic catalysis.' It has recently been suggested' that this is true only for reactions in aqueous solvents, and that in nonaqueous solvents -and perhaps also in enzyme active sites fro
β¦ LIBER β¦
On the importance of orientation in general base catalysis by carboxylate
β Scribed by Richard David Gandour
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- English
- Weight
- 555 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0045-2068
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
The efficiency of intramolecular general
β
Anthony J. Kirby; Koh Lip Lin
π
Article
π
1978
π
Elsevier Science
π
French
β 114 KB
Theoretical basis for the detection of g
β
Lee E. Kirsch; Robert E. Notari
π
Article
π
1984
π
John Wiley and Sons
π
English
β 440 KB
General base catalysis in the decomposit
β
Ll Abia; X. L. Armesto; M. Canle L.; M. V. GarcΓa; M. Losada; J. A. Santaballa
π
Article
π
1994
π
John Wiley and Sons
π
English
β 565 KB
This article analyzes the kinetics of the decomposition of N-C1-Valine in aqueous solution, which is formed rapidly by chlorination of Valine with sodium hypochlorite. A general-base catalyzed process not yet described is reported. The experimental evidence shows two competitive decomposition paths:
Intramolecular general-base- catalysis o
β
W. Tagaki; M. Ochiai; S. Oae
π
Article
π
1968
π
Elsevier Science
π
French
β 188 KB
ChemInform Abstract: Catalysis by Gold D
β
Juan C. Fierro-Gonzalez; Bruce C. Gates
π
Article
π
2008
π
John Wiley and Sons
β 23 KB
π 1 views
Rate enhancement by catalytic groups in
β
Michael J. Boland; Michael J. Hardman; Ian D. Watson
π
Article
π
1974
π
Elsevier Science
π
English
β 509 KB