Stille coupling approaches to the stereospecific synthesis of 7-[(E)-alkylidene]cephalosporins
โ Scribed by John D. Buynak; Venkata Ramana Doppalapudi; Mohammed Frotan; Ramon Kumar
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 213 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
โฆ Synopsis
Stille coupling methodology is used to stereospecifically synthesize 7-[(E)-alkylidene]cephalosporins, potential enzyme inhibitors which are unavailable via other synthetic methodology. Two procedures are described, utilizing either a stannylalkylidene cephem which is then coupled with an organohalide, or a haloalkylidene cephem which is coupled with an organostannane.
๐ SIMILAR VOLUMES
The 16-membered macrodiolide 4, corresponding to the macrocyclic core of elaiophylin (1), was prepared via the copper-mediated cyclodimerisation of stannane 3.
## Abstract The synthesis of ethyl (2__E__, 4__E__, 8__R__)โ8โmethylโ10โ[(2__H__โtetrahydropyranโ2โyl)oxy]โ2,4โdecadienoate (**11**), methyl (2__E__, 8__R__)โ8โmethylโ10โ[(2__H__โtetrahydropyranโ2โyl)oxy]โ2โdecenoate (**16**), synthons for the construction of the macrocyclic moieties of the cytocha
## Abstract For Abstract see ChemInform Abstract in Full Text.