𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Stereoselective synthesis of the bicyclic core structure of the highly oxidised sesquiterpene neoliacinic acid

✍ Scribed by J.Stephen Clark; Alexander G. Dossetter; William G. Whittingham


Book ID
103410662
Publisher
Elsevier Science
Year
1996
Tongue
French
Weight
244 KB
Volume
37
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


ChemInform Abstract: Stereoselective Con
✍ J. Stephen Clark; Carl A. Baxter; Alexander G. Dossetter; Stephane Poigny; Jose πŸ“‚ Article πŸ“… 2008 πŸ› John Wiley and Sons βš– 18 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

A model synthesis of the bicyclic core s
✍ Mauricio Gomes Constantino; Adilson Beatriz; Gil Valdo JosΓ© da Silva πŸ“‚ Article πŸ“… 2000 πŸ› Elsevier Science 🌐 French βš– 129 KB

A bicyclo[6.2.1]undecane structure, a model for the core structure of several biologically active furanoheliangolide sesquiterpenes, was synthesized through a retroΒ±aldol reaction from a tricyclo-[6.2.1.0 2,7 ]undecane. The required tricyclic compound was prepared by a DielsΒ±Alder reaction followed

Stereoselective Synthesis of the Core St
✍ Zhang, Hong ;Wang, Yali ;ThΓΌrmer, RenΓ© ;Meisenbach, Mark ;Voelter, Wolfgang πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 742 KB

## Abstract A new strategy for the construction of the __O__‐glycoside bond in the nephritogenoside unit using the phenylsulfenyl method is reported. The readily accessible phenylsulfinyl glycoside proved to be an excellent glycosyl donor, leading to high yields and good selectivity. The extremely