A practical route for enantioselective total synthesis of (+)-11-deoxy-19-norcorticosterone via intramolecular Diels-Alder addition to an ortho-quinodimethane
- Author
- NEMOTO, H; SATOH, A; ANDO, M; FUKUMOTO, K
Tohoku univ., pharmaceutical inst., Sendai 980, Japan - Source
Journal of the Chemical Society. Perkin transactions. I. 1991, Num 5, pp 1309-1314 ; ref : 9 ref
- CODEN
- JCPRB4
- ISSN
- 0300-922X
- Scientific domain
- Biochemistry, molecular biology, biophysics; Organic chemistry
- Publisher
- Royal Society of Chemistry, Cambridge
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Addition Diels Alder Corticostéroïde Cétol Enantiomère(+) Enantiosélectivité Enone Réaction intramoléculaire Stéroïde Synthèse totale 19-Norprégn-4-ène-3,20-dione(21-hydroxy)
- Keyword (en)
- Diels Alder addition Corticosteroid Ketol Enantiomer(+) Enantioselectivity Enone Intramolecular reaction Steroid Total synthesis
- Keyword (es)
- Adición Diels Alder Corticoesteroide Cetol Enantiómero (+) Enantioselectividad Enona Reacción intramolecular Esteroide Síntesis total
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C05 Alicyclic compounds, terpenoids, prostaglandins, steroids / 001C03C05D Steroids
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 4953755
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
10.1039/P19910001309 
https://dx.doi.org/10.1039/P19910001309
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