𝔖 Bobbio Scriptorium
✦   LIBER   ✦

1,3-Dithian-2-ylmethyl esters as two-step carboxy-protecting groups in the synthesis of N-glycopeptides

✍ Scribed by Waldmann, Herbert; Kunz, Horst

Book ID
126295142
Publisher
American Chemical Society
Year
1988
Tongue
English
Weight
493 KB
Volume
53
Category
Article
ISSN
0022-3263

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

ChemInform Abstract: Comparative Lipase-
ChemInform Abstract: Comparative Lipase-Catalyzed Hydrolysis of Ethylene Glycol Derived Esters. The 2-Methoxyethyl Ester as a Protective Group in Peptide and Glycopeptide Synthesis.
✍ M. GEWEHR; H. KUNZ πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 40 KB πŸ‘ 1 views

Comparative Lipase-Catalyzed Hydrolysis of Ethylene Glycol Derived Esters. The 2-Methoxyethyl Ester as a Protective Group in Peptide and Glycopeptide Synthesis. -The 2-methoxyethyl ester group is found to be a potent protecting group in the synthesis of various peptides and glycopeptides. It can be

ChemInform Abstract: 3-Benzoyl-2-ethoxyc
ChemInform Abstract: 3-Benzoyl-2-ethoxycarbonylvinyl-1 and 2-Benzoylamino-2- methoxycarbonylvinyl-1 as N-Protecting Groups in Peptide Synthesis. Their Application in the Synthesis of Dehydropeptide Derivatives Containing N-Terminal 3-Heteroarylamino-2,3-dehydroalanine.
✍ J. SVETE; M. ALJAZ-ROZIC; B. STANOVNIK πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 31 KB πŸ‘ 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 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