Synthesis of a compound having the essential structural unit for the hetisine-type of aconite alkaloids
β Scribed by Hideaki Muratake; Mitsutaka Natsume
- Publisher
- Elsevier Science
- Year
- 2002
- Tongue
- French
- Weight
- 102 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
A hexacyclic compound 1, which carries an almost full structure of the hetisine skeleton lacking only the six-membered ring with an exo methylene group, was synthesized by applying an acetal-ene reaction on 5 for the bond formation of C-14 and C-20 as well as stereoselective hydrocyanation reaction on 7 for construction of the azabicyclo ring system.
π SIMILAR VOLUMES
## Abstract The structure of neohobartine (**3**), a side product of the acidβcatalyzed conversion of (β)βhobartine (**1**) into (+)βaristoteline (**2**), has been elucidated by spectroscopic methods. Possible mechanistic pathways leading to its 1βazaaadamantane skeleton are discussed.
## Abstract magnified image A short synthesis of the hexahydropyrido[4,3β__b__]carbazole derivative **8** which is important for the preparation of aspidosperma alkaloids was described. Construction of the tetracyclic structure was achieved __via__ a short synthetic route and some new carbazolone
## 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.