Concise synthesis of guanidine-containing heterocycles using the biginelli reaction
- Author
- NILSSON, Bradley L1 ; OVERMAN, Larry E1
[1] Department of Chemistry, 1102 Natural Sciences II, University of California, Irvine, California 92697-2025, United States - Source
Journal of organic chemistry. 2006, Vol 71, Num 20, pp 7706-7714, 9 p ; ref : 33 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)
- Acide carboxylique Alcaloïde Aldéhyde Aminolyse Clivage Cétoester Déprotection Guanidines Hétérocycle azote Imine Milieu acide Protection Pyrazole dérivé Pyrimidine dérivé Structure moléculaire Synthèse chimique 5,6,8b-Triazaacénaphtylène dérivé Batzelladine Crambescidine Dispiro[oxépane-2:4'-5,6,8b-triazaacénaphtylène-7':2″-pyrane] dérivé
- Keyword (en)
- Carboxylic acid Alkaloid Aldehyde Aminolysis Cleavage Ketoester Deprotection Guanidines Nitrogen heterocycle Imine Acid medium Protection Pyrazole derivatives Pyrimidine derivatives Molecular structure Chemical synthesis
- Keyword (es)
- Acido carboxílico Alcaloide Aldehído Aminolisis Clivaje Cetoester Desprotección Guanidinas Heterociclo nitrógeno Imina Medio ácido Protección Pirazol derivado Pirimidina derivado Estructura molecular Síntesis química
- 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
- 18154474
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/jo061199m 
https://dx.doi.org/10.1021/jo061199m
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