trans-3-n-propyl-L-proline is a highly favorable, conformationally restricted replacement for methionine in the C-terminal tetrapeptide of cholecystokinin. Stereoselective synthesis of 3-allyl- and 3-n-propyul-L-proline derivatives from 4-hydroxy-L-proline
- Author
- HOLLADAY, M. W; LIN, C. W; MAY, C. S; GARVEY, D. S; WITTE, D. G; MILLER, T. R; WOLFRAM, C. A. W; NADZAN, A. M
Pharmaceutical Discovery Abbott Laboratories, neurosci. res. div., Abbott Park IL 60064, United States - Source
Journal of medicinal chemistry (Print). 1991, Vol 34, Num 1, pp 455-457, 3 p ; ref : 24 ref
- CODEN
- JMCMAR
- ISSN
- 0022-2623
- Scientific domain
- Pharmacology drugs
- Publisher
- American Chemical Society, Washington, DC
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Composé allylique Hétérocycle azote Stéréosélectivité α-Aminoacide Proline(«3»-allyl) Proline(«3»-propyl)
- Keyword (en)
- Allylic compound Nitrogen heterocycle Stereoselectivity α-Aminoacid
- Keyword (es)
- Compuesto alílico Heterociclo nitrógeno Estereoselectividad α-Aminoácido
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06B Heterocyclic compounds with only one n hetero atom and condensed derivatives
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 19614686
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1021/jm00105a068 
https://dx.doi.org/10.1021/jm00105a068
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Base Search access
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