## Abstract Syntheses of novel 16βmembered macrocyclic peptidomimetics are reported, which employ iterative peptide coupling followed by high yielding ringβclosing metathesis (RCM) as the key cyclization step. The target macrocyclic compounds include examples containing a (2__S__)βaminoβ8βoxodecano
Ring Closing Metathesis in the Synthesis of Biologically Interesting Peptidomimetics, Sugars and Alkaloids
β Scribed by William H. C. Martin; Siegfried Blechert
- Publisher
- John Wiley and Sons
- Year
- 2006
- Weight
- 8 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
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, please click on HTML or PDF.
π SIMILAR VOLUMES
The application of the ring-closing metathesis (RCM) castanospermine ( ) is presented. The utilisation of two RCM steps in the synthetic sequence leading to the multicyclic reaction to the construction of a wide variety of nitrogencontaining ring systems is described. The examples include ABCDE nucl
## 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, please click on HTML or PDF.