Dilithiated vicinal diester route to sesquiterpenes. Total synthesis of (±)-vetiselinene and the formal synthesis of other eudesmane sesquiterpenes
- Author
- GARRATT, P. J1 ; PORTER, J. R
[1] Univ. coll. London, dep. chemistry, London WC1H 0AJ, United Kingdom - Source
Journal of organic chemistry. 1986, Vol 51, Num 26, pp 5450-5452 ; ref : 21 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)
- Composé bicyclique Composé insaturé Composé monocyclique Cyclisation Diester Epoxydation Hydrocarbure Lithiation Racémique Sesquiterpène Cyclohexène-3dicarboxylique-1,2 acide,ester diméthyle Endesmane dérivé Vétisélinène
- Keyword (en)
- Bicyclic compound Unsaturated compound Monocyclic compound Cyclization Diester Epoxidation Hydrocarbon Lithiation Racemate Sesquiterpenes
- Keyword (es)
- Compuesto bicíclico Compuesto insaturado Compuesto monocíclico Ciclizacion Diester Epoxidacion Hidrocarburo Litiación Racémico Sesquiterpeno
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C05 Alicyclic compounds, terpenoids, prostaglandins, steroids / 001C03C05B Terpenoids
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 8213509
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/jo00376a084 
https://dx.doi.org/10.1021/jo00376a084
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