ChemInform Abstract: Synthesis of Constrained α-Amino Acid Derivatives via Enyne Metathesis Reaction.
✍ Scribed by S. KOTHA; N. SREENIVASACHARY; E. BRAHMACHARY
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 36 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
✦ Synopsis
Synthesis of Constrained α-Amino Acid Derivatives via Enyne Metathesis Reaction.
-Ring-closing metathesis of the enyne (VI), prepared following an optimized approach, in the presence of Grubb's catalyst gives the vinylcyclopentene (VII). The latter undergoes Diels-Alder reaction with the appropriate dienophiles. Following DDQ-oxidation of the [4 + 2] cycloadducts leads to constrained α-amino acid derivatives. -(KOTHA, S.;
📜 SIMILAR VOLUMES
## 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