Synthetic approaches and total synthesis of natural zoapatanol
- Author
- TAILLIER, Catherine1 ; GILLE, Barbara1 ; BELLOSTA, Véronique1 ; COSSY, Janine1
[1] Laboratoire de Chimie Organique, associé au CNRS, ESPCI, 10 rue Vauquelin, 75231 Paris, France - Source
Journal of organic chemistry. 2005, Vol 70, Num 6, pp 2097-2108, 12 p ; ref : 37 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 insaturé Cyclisation Enantiosélectivité Enol éther Hétérocycle oxygène Métathèse Oléfination Réaction Horner Emmons Réaction intramoléculaire Synthèse chimique Synthèse totale Dihydroxylation Sharpless Non-2-én-5-one(2,6-diméthyl-9-[3-hydroxy-6-[2-hydroxy-éthylidène]-2-methyl-oxepan-2-yl]) Oxépane dérivé Zoapatanol
- Keyword (en)
- Unsaturated compound Cyclization Enantioselectivity Enol ether Oxygen heterocycle Metathesis Olefination Horner Emmons reaction Intramolecular reaction Chemical synthesis Total synthesis
- Keyword (es)
- Compuesto insaturado Ciclización Enantioselectividad Enol eter Heterociclo oxígeno Metatesis Olefinación Reacción Horner Emmons Reacción intramolecular Síntesis química Síntesis total
- 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
- 16617302
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/jo048115z 
https://dx.doi.org/10.1021/jo048115z
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