Syntheses of Papyracillic Acids: Application of the Tandem Chain Extension―Acylation Reaction
- Author
- MAZZONE, Jennifer R1 ; ZERCHER, Charles K1
[1] Department of Chemistry, University of New Hampshire, Durham, New Hampshire 03824, United States - Source
Journal of organic chemistry. 2012, Vol 77, Num 20, pp 9171-9178, 8 p ; ref : 27 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)
- Acylation Allongement chaîne Carbénoïde Composé naturel Groupe fonctionnel Hétérocycle oxygène Réaction tandem Spirane Synthèse chimique Zinc 1,6-Dioxaspiro[4.4]non-3-ène dérivé Acide papyracillique Métal transition
- Keyword (en)
- Acylation Chain elongation Carbenoid Natural compound Functional group Oxygen heterocycle Tandem reaction Spiran Chemical synthesis Zinc Transition metal
- Keyword (es)
- Acilación Alargamiento cadena Carbenoide Compuesto natural Grupo funcional Heterociclo oxígeno Reacción tándem Espirano Síntesis química Zinc Metal transición
- 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
- 26603345
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/jo3017617 
https://dx.doi.org/10.1021/jo3017617
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