Total synthesis of (±)-dihydropinidine, (±)-monomorine I, and (±)-indolizidine 223AB (gephyrotoxin 223AB) by intramolecular nitroso Diels-Alder reaction
- Author
- WATANABE, Y1 ; IIDA, H; KIBAYASHI, C
[1] Tokyo coll. pharmacy, Hachioji, Tokyo 192-03, Japan - Source
Journal of organic chemistry. 1989, Vol 54, Num 17, pp 4088-4097 ; ref : 26 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)
- Addition Diels Alder Alcaloïde Composé bicyclique Cycle 6 chaînons Hétérocycle azote angulaire Hétérocycle azote Racémique Réaction intramoléculaire Régiosélectivité Stéréosélectivité Acide alcadiène-«5,7»carbohydroxamique Ammonium(tétrapropyl) periodate Indolizidine(butyl-3 méthyl-«5») Indolizidine(butyl-«3» propyl-«5») Pinidine(dihydro) Pipéridine dérivé
- Keyword (en)
- Diels Alder addition Alkaloid Bicyclic compound Six membered ring Angular nitrogen heterocycle Nitrogen heterocycle Racemate Intramolecular reaction Regioselectivity Stereoselectivity
- Keyword (es)
- Adición Diels Alder Alcaloide Compuesto bicíclico Ciclo 6 eslabones Heterociclo nitrógeno angular Heterociclo nitrógeno Racémico Reacción intramolecular Regioselectividad Estereoselectividad
- 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
- 7332872
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/jo00278a020 
https://dx.doi.org/10.1021/jo00278a020
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