A novel stereospecific rearrangement of 3-substituted B-homo-5-azasteroid lactams to A-nor analogues
- Author
- BACK, T. G; CHAU, J. H.-L; MORZYCKI, J. W
Univ. Calgary, dep. chemistry, Calgary AB T2N 1N4, Canada - Source
Tetrahedron letters. 1991, Vol 32, Num 45, pp 6517-6520 ; ref : 9 ref
- CODEN
- TELEAY
- ISSN
- 0040-4039
- Scientific domain
- Biochemistry, molecular biology, biophysics; Organic chemistry
- Publisher
- Elsevier, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Alcool primaire Composé tétracyclique Contraction cycle Hétérocycle azote angulaire Lactame Stéroïde Stéréospécificité Transposition chimique 4-Aza-4-nor-β-homo-androstan-5-one(17-benzyloxy-3-chlorométhyl) 5-Aza-β-homo-androstan-6-one(17-benzyloxy-3-hydroxy) Azastéroïde
- Keyword (en)
- Primary alcohol Tetracyclic compound Ring contraction Angular nitrogen heterocycle Lactam Steroid Stereospecificity Chemical rearrangement Azasteroide
- Keyword (es)
- Alcohol primario Compuesto tetracíclico Contracción ciclo Heterociclo nitrógeno angular Lactamo Esteroide Estereoespecificidad Transposición química
- 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
- 5103476
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
10.1016/0040-4039(91)80208-N 
https://dx.doi.org/10.1016/0040-4039(91)80208-N
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