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Malic acid: A convenient precursor for the synthesis of peptide secondary structure mimetics

โœ Scribed by Hwa-Ok Kim; Chris Lum; Min S. Lee


Publisher
Elsevier Science
Year
1997
Tongue
French
Weight
155 KB
Volume
38
Category
Article
ISSN
0040-4039

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๐Ÿ“œ SIMILAR VOLUMES


ChemInform Abstract: Malic Acid: A Conve
โœ H.-O. KIM; C. LUM; M. S. LEE ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 29 KB ๐Ÿ‘ 2 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 โ€œFull Textโ€ option. The original article is trackable v

The use of ฮณ-turn mimetics to define pep
โœ James F. Callahan; Kenneth A. Newlander; Joelle L. Burgess; Drake S. Eggleston; ๐Ÿ“‚ Article ๐Ÿ“… 1993 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 803 KB

A novel ytum mimetic 2 has been prepared based on retro amide peptide design Incorporation of this mimetic into linear peptidejibritwgen receptor antagonist 7 (GPlIWIUa receptor) @rds the opportunity to test models of antagonist pharmacophore.

A New Convenient Route for the Synthesis
โœ Nakonieczna, Lucja ;Przychodzeล„, Witold ;Chimiak, Andrzej ๐Ÿ“‚ Article ๐Ÿ“… 1994 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 436 KB

## Abstract The __tert__โ€butyldimethylsilyl group as the catechol protective group of DOPA (compound 1a), Bocโ€DOPA (compound 1b) and DOPA esters (compounds 2aโ€“c) is introduced. The compounds 2aโ€“c and 1b are used as the starting substrates for the synthesis of the protected __N__โ€terminal DOPA and _