Intramolecular nucleophilic amino attack in a monobactam: synthesis and stability of (2S,3S)-3-[(2R)-2-amino-2-phenylacetamido]-2-methyl-4-oxo-1-azetidinesulfonic acid
- Author
- INDELICATO, J. M1 ; FISHER, J. W; PASINI, C. E
[1] Eli Lilly co., Indianapolis IN 46285, United States - Source
Journal of pharmaceutical sciences. 1986, Vol 75, Num 3, pp 304-306 ; ref : 11 ref
- CODEN
- JPMSAE
- ISSN
- 0022-3549
- Scientific domain
- Pharmacology drugs
- Publisher
- American Pharmaceutical Association, Washington, DC
/
Wiley, Hoboken, NJ
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Carboxamide Cycle 4 chaînons Hétérocycle azote Lactame Spectre IR Spectre RMN Azétidinesulfonique-1 acide(méthyl-4 oxo-«2» phénylglycylamino-«3») Carbone 13 Hydrogène 1
- Keyword (en)
- Carboxamide Four membered ring Nitrogen heterocycle Lactam Infrared spectrum NMR spectrum
- Keyword (es)
- Carboxamida Ciclo 4 eslabones Heterociclo nitrógeno Lactamo Espectro IR Espectro de RMN
- 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
- 7921076
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
10.1002/jps.2600750321 
https://dx.doi.org/10.1002/jps.2600750321
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