Novel thermal and microwave-assisted facile route to naphthalen-2(1 h)-ones via an oxidative alkoxylation-ringopening protocol

Organic Letters

Volumn 11, Issue 14, 2009, Pages 2964-2967

  Dolka, Chrysanthi ^a   Van Hecke, Kristof ^b   Van Meervelt, Luc ^b   Tsoungas, Petros G ^c   Van Der Eycken, Erik V ^b   Varvounis, George ^a  

^a UNIVERSITY OF IOANNINA   (Greece)

^b UNIVERSITY OF LEUVEN   (Belgium)

^c Ministry of Development   (Greece)

Author keywords

[No Author keywords available]

Indexed keywords

NAPHTHOL DERIVATIVE; OXIME;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; COMBINATORIAL CHEMISTRY; MICROWAVE RADIATION; OXIDATION REDUCTION REACTION; SYNTHESIS;

CATALYSIS; COMBINATORIAL CHEMISTRY TECHNIQUES; MICROWAVES; MOLECULAR STRUCTURE; NAPHTHOLS; OXIDATION-REDUCTION; OXIMES;

EID: 67650283718     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol9008574     Document Type: Article

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48. CCDC-725437 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge via www.cam.ac.uk/ conts/retrieving.html (or from the Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, UK; fax: (+44-1223-336033; or deposit@ccdc.cam.uk).