?-Peptides Forming More Stable Secondary Structures than ?-Peptides: Synthesis and helical NMR-solution structure of the ?-hexapeptide analog of H-(Val-Ala-Leu)2-OH-Reference-Cited by-同舟云学术

?-Peptides Forming More Stable Secondary Structures than ?-Peptides: Synthesis and helical NMR-solution structure of the ?-hexapeptide analog of H-(Val-Ala-Leu)2-OH

Published:1998 Issue:5-8 Volume:81 Page:983-1002
ISSN:0018-019X
Container-title:Helvetica Chimica Acta
language:de
Short-container-title:Helv. Chim. Acta

Author:

Hintermann Tobias,Gademann Karl,Jaun Bernhard,Seebach Dieter

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis

Reference46 articles.

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3. ?2- and ?3-Peptides with Proteinaceous Side Chains: Synthesis and solution structures of constitutional isomers, a novel helical secondary structure and the influence of solvation and hydrophobic interactions on folding

4. in ?Houben-Weyl: Stereoselective Synthesis?, Eds. and Georg Thieme Verlag, Stuttgart-New York, 1996, Chapt. 1.

5. Beitrag zur asymmetrischen Synthese bicyclischer Verbindungen unter Katalyse mit optisch aktiven Aminosäuren. Synthese von (S)-2-Pyrrolidin-propionsäure und (R)-4-Amino-5-phenylvaleriansäure

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