๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

A total synthesis of dl-velbanamine

โœ Scribed by Masayuki Narisada; Fumihiko Watanabe; Wataru Nagata


Publisher
Elsevier Science
Year
1971
Tongue
French
Weight
228 KB
Volume
12
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

โœฆ Synopsis


Velbanamine wconstitutes the tetmcyclic indole moiety of the dimeric alkaloids, vinblastine wand vincristine &) (l), and wos obtained during structure elucidation studies(lq2)on the latter alkaloids. The reported syntheses of&, a potentiol intermediate for the preparation of the oncolytic alkaloids w and (2&),


๐Ÿ“œ SIMILAR VOLUMES


Total synthesis of dl-elemol
โœ E.J. Corey; Emil A. Broger ๐Ÿ“‚ Article ๐Ÿ“… 1969 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 238 KB
A new total synthesis of dl-sirenin
โœ T. Mandai; K. Hara; M. Kawada; J. Nokami ๐Ÿ“‚ Article ๐Ÿ“… 1983 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 118 KB
First total synthesis of dl-duocarmycin
โœ Yasumichi Fukuda; Kazuhiko Nakatani; Yoshio Ito; Shiro Terashima ๐Ÿ“‚ Article ๐Ÿ“… 1990 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 228 KB
Total synthesis of dl-corynantheine
โœ E.E. van Tamelen; I.G. Wright ๐Ÿ“‚ Article ๐Ÿ“… 1964 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 217 KB
Total synthesis of dl-pederamide
โœ Kazuo Tsuzuki; Takahiro Watanabe; Mitsutoshi Yanagiya; Takeshi Matsumoto ๐Ÿ“‚ Article ๐Ÿ“… 1976 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 191 KB

We report here a stereochemically controlled total synthesis of pederamide 11) , a main hydrolysis product of the structurally unique and powerful insect C poison pederin z), in dl-form.