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Total synthesis of the germacranolide (±)-aristolactone via [2,3] Wittig ring contraction

Author
MARSHALL, J. A1 ; LEBRETON, J; DEHOFF, B. S; JENSON, T. M
[1] Univ. South Carolina, dep. chemistry, Columbia SC 29208, United States
Source

Tetrahedron letters. 1987, Vol 28, Num 7, pp 723-726 ; 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)
Alcool secondaire Composé aliphatique Composé bicyclique Composé diénique Composé insaturé Composé énynique Cyclisation Ester Lactone Macrocycle Monoterpène Racémique Réactif Grignard Sesquiterpène Transposition Wittig Aristolactone Cyclodécène-6yne-«2»ol(isopropényl-«10» méthyl-«7») Germacranolide Géraniol,acétate
Keyword (en)
Secondary alcohol Aliphatic compound Bicyclic compound Dienic compound Unsaturated compound Enynic compound Cyclization Ester Lactone Macrocycle Monoterpene Racemate Grignard reagent Sesquiterpenes Wittig rearrangement
Keyword (es)
Alcohol secundario Compuesto alifatico Compuesto bicíclico Compuesto diénico Compuesto insaturado Compuesto enínico Ciclizacion Ester Lactona Macrociclo Monoterpeno Racémico Reactivo Grignard Sesquiterpeno Transposición Wittig
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
8237567

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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