## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
Pd(II)—dppb and syngas catalyze regioselective hydroesterification of terminal alkynes under neutral conditions
✍ Scribed by Bassam El Ali; Jimoh Tijani; Abdel Moneim El-Ghanam
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- French
- Weight
- 63 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Palladium(II) regioselectively catalyzes the hydroesterification of terminal alkynes under syngas forming a,b-unsaturated esters 3 and 4 in excellent chemical yields under neutral conditions. The high selectivity for the linear ester 4 was obtained with a catalytic system that includes Pd(II), 1,4-bis(diphenylphosphino)butane (dppb) and CO/H 2 in CH 2 Cl 2 as solvent. The control of the regioselectivity depends strongly upon the type of ligand, the solvent and the use of the syngas mixture.
📜 SIMILAR VOLUMES
The carbonylative coupling of aniline derivatives (1a±h) with terminal aryl acetylenes (2a, b) catalyzed by Pd(OAc) 2 and 1,4-bis(diphenylphosphino)butane (dppb) under syngas conditions aords acrylamide derivatives 3 or 3 H in excellent yields and selectivities.
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v