𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Total Synthesis of Proposed Amphidinolide A via a Highly Selective Ring-Closing Metathesis

✍ Scribed by Maleczka,, Robert E.; Terrell, Lamont R.; Geng, Feng; Ward, Joseph S.


Book ID
120200634
Publisher
American Chemical Society
Year
2002
Tongue
English
Weight
99 KB
Volume
4
Category
Article
ISSN
1523-7060

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Total synthesis of octalactin A via ring
✍ Keith R Buszek; Nagaaki Sato; Youngmee Jeong πŸ“‚ Article πŸ“… 2002 πŸ› Elsevier Science 🌐 French βš– 93 KB

A new total synthesis of the novel lactone natural product octalactin A is described. The key step involves the facile construction of the eight-membered lactone core via ring-closing metathesis (RCM). This oxocene was elaborated to give the powerful antitumor agent octalactin A.

Total synthesis of (βˆ’)- and (Β±)-frontali
✍ Matthias Scholl; Robert H. Grubbs πŸ“‚ Article πŸ“… 1999 πŸ› Elsevier Science 🌐 French βš– 215 KB

Racemic and enantiopure targets containing the 6,8-dioxabicycio [3.2.1]octane skeleton, can be conveniently synthesized from monocyclic diene precursors using an intramolecular ruthenium-catalyzed ring-closing metathesis reaction as the key step.

ChemInform Abstract: Total Synthesis of
✍ Keith R. Buszek; Nagaaki Sato; Youngmee Jeong πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 29 KB πŸ‘ 2 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 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