The importance of vinylsilane stereochemistry and σ-π stabilization in iminium ion-vinylsilane cyclizations. A short total synthesis of the Amaryllidacea alkaloids (±)-epielwesine
- Author
- OVERMAN, L. E1 ; BURK, R. M
[1] Univ. California, dep. chemistry, Irvine CA 92717, United States - Source
Tetrahedron letters. 1984, Vol 25, Num 50, pp 5739-5742 ; ref : 12 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)
- Alcaloïde Composé aromatique Composé bicyclique Composé pentacyclique Enantiomère(+) Epimère Hydratation Hétérocycle azote Hétérocycle oxygène azote Réaction Pictet Spengler Silicium Composé organique Stéréoisomère Benzodioxole-1,3acétonitrile-5 Elwésine Ethano dioxolo phénanthridine dérivé Indoline(phényl-3 tétrahydro-3a,4,5,7a) Indolinol-6([benzodioxole-1,3yl-5]-3a perhydro) Pyrroline-1([benzodioxole-1,3yl-5]-3a triméthylsilyl-4p butène-3p yl-3) Pyrroline-1(phényl-3 triméthylsilyl-4p butène-3p yl-3)
- Keyword (en)
- Alkaloid Aromatic compound Bicyclic compound Pentacyclic compound Enantiomer(+) Epimer Hydration Nitrogen heterocycle Oxygen nitrogen heterocycle Pictet Spengler reaction Silicon Organic compounds Stereoisomer
- Keyword (es)
- Alcaloide
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06D Heterocyclic compounds with n hetero atom and also o and/or s, se, te hetero atoms
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 8916240
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/S0040-4039(01)81674-9 
https://dx.doi.org/10.1016/S0040-4039(01)81674-9
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