𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Tandem aza-Claisen rearrangement and ring-closing metathesis reactions: the stereoselective synthesis of functionalised carbocyclic amides

✍ Scribed by Michael D. Swift; Adele Donaldson; Andrew Sutherland

Book ID
108285411
Publisher
Elsevier Science
Year
2009
Tongue
French
Weight
397 KB
Volume
50
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

ChemInform Abstract: A Tandem Aza-Claise
ChemInform Abstract: A Tandem Aza-Claisen Rearrangement and Ring Closing Metathesis Reaction for the Synthesis of Cyclic Allylic Trichloroacetamides.
✍ Michael D. Swift; Andrew Sutherland πŸ“‚ Article πŸ“… 2008 πŸ› John Wiley and Sons βš– 45 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

Efficient synthesis of novel carbocyclic
Efficient synthesis of novel carbocyclic nucleosides via sequential Claisen rearrangement and ring-closing metathesis
✍ Ok Hyun Ko; Joon Hee Hong πŸ“‚ Article πŸ“… 2002 πŸ› Elsevier Science 🌐 French βš– 72 KB

Very efficient synthetic route to novel 4%a-C-hydroxymethyl branched carbocyclic nucleosides was described. The stereocontrolled synthesis of target nucleosides was successfully achieved by Johnson orthoester-Claisen rearrangement, ring-closing metathesis (RCM) starting from a simple acyclic precurs