## 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 βFull Textβ option. The original article is trackable v
Enantioselective total synthesis of natural 11,12-epoxycembrene-C
β Scribed by Yulin Li; Zuosheng Liu; Jiong Lan; Jing Li; Lizeng Peng; Weidong Z Li; Ying Li; Albert S.C Chan
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- French
- Weight
- 120 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
The first enantioselective total synthesis of (+)-11,12-epoxycembrene-C (1), a novel naturally occurring cembranoxide isolated from tropical marine soft coral, was achieved via a general approach by employing an intramolecular McMurry coupling and Sharpless asymmetric epoxidation as key steps from readily available starting materials.
π SIMILAR VOLUMES
## Abstract The naturally occurring Lycopodium alkaloid (+)βluciduline (**1**) has been synthesized from (__R__)β5βmethylβcyclohexβ2βenβ1βone (**12**) by a sequence of seven steps (s. __Scheme 6__) in 33% overall yield. The key step **4β6** presumably involves a transient nitrone **5** which underg
## 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 βFull Textβ option. The original article is trackable v