Synthesis of carbazoles via an intramolecular cyclization of 2-(6-substituted 3(Z)-hexen-1,5-diynyl)anilines and their related molecules
- Author
- LEE, Chia-Ying1 ; LIN, Chi-Fong2 ; LEE, Jeng-Lin1 ; CHIU, Ching-Chen2 ; LU, Wen-Der1 ; WU, Ming-Jung2
[1] Graduate Institute of Pharmaceutical Sciences, Kaohsiung Medical University, Kaohsiung, Taiwan, Province of China
[2] Faculty of Medicinal and Applied Chemistry, Kaohsiung Medical University, Kaohsiung, Taiwan, Province of China - Source
Journal of organic chemistry. 2004, Vol 69, Num 6, pp 2106-2110, 5 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)
- Acétamide Aniline dérivé Carbazole dérivé Composé acétylénique Composé diynique Composé énynique Composé éthylénique Cyclisation Hétérocycle azote Indole dérivé Réaction intramoléculaire Synthèse chimique Potassium [3-éthyl]pentanolate Potassium t-butanolate
- Keyword (en)
- Acetamide Aniline derivatives Carbazole derivatives Acetylenic compound Diynic compound Enynic compound Ethylenic compound Cyclization Nitrogen heterocycle Indole derivatives Intramolecular reaction Chemical synthesis
- Keyword (es)
- Acetamida Anilina derivado Carbazol derivado Compuesto acetilénico Compuesto diínico Compuesto enínico Compuesto etilénico Ciclización Heterociclo nitrógeno Indol derivado Reacción intramolecular Síntesis química
- 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
- 15611360
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/jo0303158 
https://dx.doi.org/10.1021/jo0303158
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