A straightforward approach towards cyclic peptides via ring-closing metathesis?scope and limitations
โ Scribed by Kazmaier, Uli; Hebach, Christina; Watzke, Anja; Maier, Sabine; Mues, Heike; Huch, Volker
- Book ID
- 119953107
- Publisher
- Royal Society of Chemistry
- Year
- 2005
- Tongue
- English
- Weight
- 429 KB
- Volume
- 3
- Category
- Article
- ISSN
- 1477-0520
- DOI
- 10.1039/B411228H
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
A strategy employing the second generation Grubbs catalyst in order to facilitate the generation of a variety of cyclic enol phosphates, including 2H-chromen-4-yl, 1,2-dihydroquinolin-4-yl, 2H-thiochromen-4-yl, 2H-thiochromen-4-yl 1,1-dioxide, and benzofuran-2-yl enol phosphate scaffolds is describe
Cyclic Sulfonamides via the Ring-Closing Metathesis Reaction. -Ring closing metathesis of various allyl-and vinylsulfonylamides in the presence of Grubb's ruthenium catalyst yields novel cyclic allyl-and vinylsultams. In the case of substrate (IX), the pyrrole (X) is formed instead of the expected