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Novel asymmetric approach to proline-derived spiro-β-lactams

Author
KHASANOV, Alisher B1 ; RAMIREZ-WEINHOUSE, Michele M2 ; WEBB, Thomas R1 ; THIRUVAZHI, Mohan1
[1] Department of Chemistry Research, ChemBridge Research Laboratories, 16981 Via Tazon, San Diego, California 92127, United States
[2] ChemBridge Corporation, 16981 Via Tazon, San Diego, California 92127, United States
Source

Journal of organic chemistry. 2004, Vol 69, Num 17, pp 5766-5769, 4 p

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)
Aminoacide Chlorure acyle Composé aromatique Composé chiral Hétérocycle azote Imine Mécanisme réaction Proline Réaction Staudinger Spirane Stéréosélectivité Synthèse asymétrique β-Lactamines 2,5-Diazaspiro[3.4]octan-1-one dérivé
Keyword (en)
Aminoacid Acyl chloride Aromatic compound Chiral compound Nitrogen heterocycle Imine Reaction mechanism Proline Staudinger reaction Spiran Stereoselectivity Asymmetric synthesis β-Lactams
Keyword (es)
Aminoácido Cloruro acilo Compuesto aromático Compuesto quiral Heterociclo nitrógeno Imina Mecanismo reacción Prolina Reacción Staudinger Espirano Estereoselectividad Síntesis asimétrica β-Lactams
Classification
Pascal
001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06C Heterocyclic compounds with several n hetero atoms in the same ring, in separated rings or in fused rings

Discipline
Organic chemistry
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
16032785

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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