𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Amide bond isosteres: Imidazolines in pseudopeptide chemistry

✍ Scribed by Raymond C.F. Jones; Gary J. Ward

Book ID
104217574
Publisher
Elsevier Science
Year
1988
Tongue
French
Weight
264 KB
Volume
29
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Microwave solvent free regioselective 1,
Microwave solvent free regioselective 1,3 dipolar cycloaddition in the synthesis of 1,4 substituted [1,2,3]-triazoles as amide bond isosteres
✍ Elisa Perissutti; Francesco Frecentese; Ferdinando Fiorino; Beatrice Severino; D πŸ“‚ Article πŸ“… 2007 πŸ› Journal of Heterocyclic Chemistry 🌐 English βš– 327 KB

## Abstract magnified image 1,3 Dipolar cycloaddition of Fmoc‐amino azides and acetylenic amides produces under solvent free irradiation a mixture of 1,4 or 1,5 substituted [1,2,3]‐triazoles. The presence of copper (I) iodide, plays a central role on regioselectivity. Four Fmoc‐amino azides charac

Synthesis of 6-alk-1β€²-enyl penicillanic
Synthesis of 6-alk-1β€²-enyl penicillanic acids; double bond isosteres of the side-chain amide linkage in penicillins
✍ Stephen A. Matlin; Lam Chan πŸ“‚ Article πŸ“… 1981 πŸ› Elsevier Science 🌐 French βš– 194 KB

Two penicillin analogues have been prepared which incorporate C=C bonds at C60 and C6B respectively, in place of the normal side-chain NHCO group. The concept of isosteric replacement of an amide function by a carbon-carbon double bond has recently been exemplified in the synthesis of active enkepha

Microwave Solvent-Free Regioselective 1,
Microwave Solvent-Free Regioselective 1,3-Dipolar Cycloaddition in the Synthesis of 1,4-Substituted[1,2,3]-triazoles as Amide Bond Isosteres.
✍ Elisa Perissutti; Francesco Frecentese; Ferdinando Fiorino; Beatrice Severino; D πŸ“‚ Article πŸ“… 2007 πŸ› John Wiley and Sons βš– 23 KB πŸ‘ 1 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, please click on HTML or PDF.