𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of the Bicyclic Dienone Core of the Antitumor Agent Ottelione B.

✍ Scribed by Derrick L. J. Clive; Stephen P. Fletcher


Publisher
John Wiley and Sons
Year
2010
Weight
31 KB
Volume
33
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Synthesis of the Bicyclic Core of Pumili
✍ Alexander Sudau; Winfried MΓΌnch; Jan-W. Bats; Udo Nubbemeyer πŸ“‚ Article πŸ“… 2002 πŸ› John Wiley and Sons 🌐 English βš– 240 KB πŸ‘ 1 views

The bicyclic core of the pumiliotoxins was synthesized in nine to eleven steps starting from L-(-)-proline. This chiral pool starting material was initially converted into an optically active 2-vinylpyrrolidine by standard operations. The first key step allowed the generation of a nine-membered ring

ChemInform Abstract: Synthesis of the Po
✍ Derrick L. J. Clive; Dazhan Liu πŸ“‚ Article πŸ“… 2008 πŸ› John Wiley and Sons βš– 19 KB πŸ‘ 2 views

## 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 of an article which was published elsewhere, please select a β€œFull Text” option. The original article is trackable v

ChemInform Abstract: The Development of
✍ R. S. COLEMAN; A. J. CARPENTER πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 33 KB πŸ‘ 2 views

The Development of Strategies for Construction of the Aziridine Core of the Antitumor Agents Azinomycins A and B. -The key steps in the synthesis of the aziridine (VII) are Wadsworth-Horner-Emmons olefination to form the derivative (III), its bromination to the (E)-isomer (IV), and cyclization of th

Structure, synthesis, and antitumor acti
✍ Wayne K. Anderson; D. Michael Houston; Mark A. Jarosinski; Frederick R. Kinder J πŸ“‚ Article πŸ“… 1993 πŸ› John Wiley and Sons 🌐 English βš– 338 KB πŸ‘ 1 views

## Abstract The two isomeric monocarbamates, 2b and 2c, related to the antitumor drug carmethizole (1) were synthesized and the structure of the carmethizole hydrolysis product, 2b, was established by X‐ray crystallography. The chemical reactivity, toxicity, and antitumor activity of the two monoca