Synthesis and conformational studies of dipeptides constrained by disubstituted 3-(aminoethoxy)propionic acid linkers
- Author
- SRINIVASA REDDY, D1 ; VANDER VELDE, David1 ; AUBE, Jeffrey1
[1] Department of Medicinal Chemistry, 1251 Wescoe Hall Drive, Malott Hall, Room 4070, University of Kansas, Lawrence, Kansas 66045-7582, United States - Source
Journal of organic chemistry. 2004, Vol 69, Num 5, pp 1716-1719, 4 p ; ref : 13 ref
- CODEN
- JOCEAH
- ISSN
- 0022-3263
- Scientific domain
- Biochemistry, molecular biology, biophysics; Organic chemistry
- Publisher
- American Chemical Society, Washington, DC
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Analyse conformationnelle Corrélation homonucléaire Dipeptide Hétérocyclisation Macrocyclisation Peptide cyclique Spectrométrie 2 dimensions Spectrométrie RMN Synthèse peptidique Hexanoïque acide(6-amino) Propionique acide(3-aminoéthoxy)
- Keyword (en)
- Conformational analysis Homonuclear correlation Dipeptides Heterocyclization Macrocyclization Cyclic peptides Two dimension spectrometry NMR spectrometry Peptide synthesis
- Keyword (es)
- Análisis conformacional Correlación homonuclear Dipéptido Heterociclización Macrociclización Péptido cíclico Espectrometría bidimensional Espectrometría RMN Síntesis peptídica
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C08 Peptides
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 16639603
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/jo035683q 
https://dx.doi.org/10.1021/jo035683q
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