## Abstract The reaction mechanism of the reduction o certain 2βbenzoylbenzoic acids and esters is discussed. It is suggested that the carboxyl group directs product formation either by neighboring group participation or by facilitating the hydrogenolysis of the carbinol group. Furthermore, it is c
The crystal structures of tributyltin and triphenyltin esters of 2-benzoylbenzoic acid
β Scribed by Lian Ee Khoo; Ngoh Khang Goh; Lip Lin Koh; Yan Xu; Sheng Luo Bao; Thomas C.W. Mak
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 263 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0277-5387
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
The triphenyltin adduct of mefenamic acid, [SnPh 3 L] (1), the monophenyltin complex [PhSnOL] n (2), and the dibutyltin complex [SnBu 2 L 2 ] (3), where HL is 2-[bis(2,3-dimethylphenyl)amino]benzoic acid (mefenamic acid), have been prepared and structurally characterized by means of vibrational, 1 H
Triphenyltin(IV) compounds of p-ethoxybenzoic acid and acetylsalicylic acid contain molecular units with Sn-O bonds and distorted tetrahedral tin centers. The phthalic acid derivative contains two four-coordinate tin atoms between which the phthalic acid unit effectively forms a bridge. The salicyla