ChemInform Abstract: Towards a Versatile Synthesis of Kainoids. Part 1. Introduction of the C-3 and C-4 Substituents.
β Scribed by J. E. BALDWIN; S. J. BAMFORD; A. M. FRYER; M. P. W. RUDOLPH; M. E. WOOD
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 32 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
β¦ Synopsis
Towards a Versatile Synthesis of Kainoids. Part 1. Introduction of the C-3 and C-4 Substituents.
-Starting from trans-4-hydroxy-Lproline, an enamine alkylation is used for the stereospecific introduction of the C-3 substituent of acromelic acid analogues. For the introduction of C-4 aryl substituents, two approaches are explored. -(BALDWIN,
π SIMILAR VOLUMES
Towards a Versatile Synthesis of Kainoids. Part 2. Two Methods for Establishment of C-4 Stereochemistry. -Starting with the compounds (I) and (IV), benzylic lactone hydrogenolysis and enamide reduction are used to generate protected C-4 aryl substituted kainoid analogues. In the last case, equal rat
## 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 βFull Textβ 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 βFull Textβ option. The original article is trackable v