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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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