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Fluoroolefin dipeptide isosteres -II. : Enantioselectlve synthesis of both antipodes of the phe-gly dlpeptide mimic

✍ Scribed by Thomas Allmendinger; Eduard Felder; Ernst Hungarbühler


Publisher
Elsevier Science
Year
1990
Tongue
French
Weight
244 KB
Volume
31
Category
Article
ISSN
0040-4039

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Fluoroolefin dipeptide isosteres — I.: T
✍ Thomas Allmendinger; Pascal Furet; Ernst Hungerbühler 📂 Article 📅 1990 🏛 Elsevier Science 🌐 French ⚖ 255 KB

The syntheses of Gly-Gly and racemic Phe-Gly fluoroolefin dipeptide isosteres are described, the firs-f examples of a new class of peptkle anabgues. The use of non-hydrolyzable amide isosteres is an established approach 12 to overcoming one of the major drawbacks in the use of peptides as therapeut