Stereocontrolled Synthesis of ψ[CH(CF3)NH]Gly-Peptides.
✍ Scribed by Marco Molteni; Alessandro Volonterio; Matteo Zanda
- Book ID
- 101955516
- Publisher
- John Wiley and Sons
- Year
- 2004
- Weight
- 48 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0931-7597
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📜 SIMILAR VOLUMES
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
## Abstract Partially modified retro‐ (PMR) and retro‐inverso (PMRI) ψ[NHCH(CF~3~)]Gly peptides, a conceptually new class of peptidomimetics, have been synthesized in wide structural diversity and variable length by aza‐Michael reaction of enantiomerically pure α‐amino esters and peptides with enan