Total synthesis of (.+-.)-N-methylmaysenine
โ Scribed by Corey, E. J.; Weigel, Leland O.; Floyd, David; Bock, Mark G.
- Book ID
- 121873176
- Publisher
- American Chemical Society
- Year
- 1978
- Tongue
- English
- Weight
- 390 KB
- Volume
- 100
- Category
- Article
- ISSN
- 0002-7863
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
The benzo[c]phenanthridine alkaloid, N-nomitidine has been synthesized employing a benzpe-VinYl isocyanate cycloaddition as the key transfomration. The tetracyclic benzo[c]phenanthridines constitute an important sub-class of the isoquinoline alkaloid family' and a number of these species have elicit
## An efficient synthesis of the colchicine degradation product N-acetylcolchinol 1 is described featuring a thallium(lIl)-mediated intramolecular non-phenolic biaryl oxidative coupling reaction of intermediate U as the key step. Both the synthetic sample and that obtained from the degradation of co