Thirty-Five Years of Synthetic Studies Directed Towards the Histrionicotoxin Family of Alkaloids
β Scribed by Alex Sinclair; Robert A. Stockman
- Publisher
- John Wiley and Sons
- Year
- 2007
- Weight
- 11 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
## 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, please click on HTML or PDF.
Synthetic Studies Towards the Indole Alkaloid Tacamine. Part 4. Total Syntheses of Tacamine-Type Indole Alkaloids of Tabernaemontana eglandulosa. -Seven alkaloids (VI)-(VIII), (XII), and (XIV)-(XVI) are prepared via epimerization of the ester (II). However, attempted synthesis of the alkaloid (Β±)-19
## Abstract According to a general concept for the total synthesis of pseurotin A (1), a secondary metabolite of __Pseudeurotium ovalis__ STOLK, 5β[(1__S__,2__S__,__Z__)β1,2βdihydroxyhexβ3βenyl]β2,2,4βtrimethylfuranβ3(2__H__)βone (17) was prepared. It is a model substance for the substituted furanβ