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The high pressure mediated intramolecular Diels-Alder reaction of furan dienes: a synthetic approach towards daphnanes

Author
BURRELL, S. J1 ; DEROME, A. E; EDENBOROUGH, M. S; HARWOOD, L. M; LEEMING, S. A; ISAACS, N. S
[1] Univ. Oxford, Dyson Perrins lab., Oxford OX1 3QY, United Kingdom
Source

Tetrahedron letters. 1985, Vol 26, Num 18, pp 2229-2232 ; ref : 13 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)
Addition Diels Alder Composé diénique conjugué Composé tricyclique Contrôle cinétique Contrôle thermodynamique Cycle 5 chaînons Diterpène Enone Haute pression Hétérocycle oxygène Méthane(dichloro) Réaction intramoléculaire Stéréochimie Benzocyclohepténone-5(époxy-3,9a octahydro-3,4,4a,6,7,8,9,9a) Daphnane dérivé Heptène-1one-3([méthyl-5 furyl-2]-7)
Keyword (en)
Diels Alder reaction Conjugated dienic compound Tricyclic compound Kinetic control Thermodynamic control Five membered ring Diterpene Enone High pressure Oxygen heterocycle Dichloromethane Intramolecular reaction Stereochemistry
Classification
Pascal
001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06A Heterocyclic compounds with o, s, se, te hetero atom and condensed derivatives

Discipline
Organic chemistry
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
9102684

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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