𝔖 Bobbio Scriptorium
✦   LIBER   ✦

An efficient one-pot access to trithiocarbonate-tethered peptidomimetics

✍ Scribed by N. Narendra; H.S. Lalithamba; Vommina V. Sureshbabu


Book ID
104098356
Publisher
Elsevier Science
Year
2010
Tongue
French
Weight
474 KB
Volume
51
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

✦ Synopsis


A simple protocol for the synthesis of a new class of trithiocarbonate-linked peptidomimetics and neoglycosylated amino acids is described. N-Protected amino alkyl thiols were treated with CS 2 in the presence of triethylamine (TEA) to generate trithiocarbonate salt, which upon reaction with appropriate halides afforded dipeptidomimetics in good yields. Further, the procedure was also extended for the synthesis of N,N 0 -orthogonally protected trithiocarbonate-linked dipeptidomimetics.


πŸ“œ SIMILAR VOLUMES


ChemInform Abstract: An Efficient, One-P
✍ Devdutt Chaturvedi; Amit K. Chaturvedi; Nisha Mishra; Virendra Mishra πŸ“‚ Article πŸ“… 2008 πŸ› John Wiley and Sons βš– 38 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

An efficient one-pot route to an aza-bri
✍ Wen-Jwu Wang; Kuo-Shen Chuang; Chi-Fong Luo; Hai-Yang Liu πŸ“‚ Article πŸ“… 2000 πŸ› Elsevier Science 🌐 French βš– 91 KB

A facile synthesis of an aza-bridged bis-1,10-phenanthroline macrocycle is described. X-ray crystallographic analysis of the aza-bridged bis-1,10-phenanthroline revealed that the two central hydrogen atoms were localized on two of the opposite central nitrogen atoms similar to those of free base por