𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A PHOTOLABILE PROTECTING GROUP FOR THE PHENOLIC HYDROXYL FUNCTION OF TYROSINE

✍ Scribed by Amit, Boaz ;Hazum, Eli ;Fridkin, Mati ;Patchornik, Abraham

Book ID
115097331
Publisher
Wiley (Blackwell Publishing)
Year
2009
Tongue
English
Weight
386 KB
Volume
9
Category
Article
ISSN
0367-8377

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

4-Nitrobenzyl group for protection of hy
4-Nitrobenzyl group for protection of hydroxyl functions
✍ Koichi Kukase; Hideo Tanaka; Sigeru Toriib; Shoichi Kusumoto πŸ“‚ Article πŸ“… 1990 πŸ› Elsevier Science 🌐 French βš– 322 KB

Versatile use of 4-nitrobenzyl group for protection of hydroxyl functions is described. It can be removed selectively in the presence of other benzyl-type protecting groups such as benzyl and 4-methoxybenzyl via reduction into 4-aminobenzyl group followed by electrochemical oxidation. Very clean o

Photolabile p-methoxyphenacyloxycarbonyl
Photolabile p-methoxyphenacyloxycarbonyl group for the protection of amines
✍ George Church; Jean-Marie Ferland; Jean Gauthier πŸ“‚ Article πŸ“… 1989 πŸ› Elsevier Science 🌐 French βš– 214 KB

P-Methoxyphenacyloxycarbonyl (Phenoc) is a new photolabile protective group for ami nes. Various phenacyl urethanes, i.e. Phenoc protected amines, have been prepared. An appli cation of the group in peptide synthesis is reported. Various protective groups for amines are known'.

A new protecting group for the carbonyl
A new protecting group for the carbonyl function
✍ E.J. Corey; E.J. Trybulski; J. William Suggs πŸ“‚ Article πŸ“… 1976 πŸ› Elsevier Science 🌐 French βš– 201 KB

During the course of various synthetic projects under study in these Laboratories we have had occasion to devise and apply a number of new methods for the protection of hydroxyl' , carbony and la&one' functions. 4 We now wish to report some recent results on the protection of aldehydes and ketones