Combined Claisen rearrangement and olefin metathesis as a route to diverse naphthalene derivatives
A new route to several medium ring heterocycle and carbocycle fused naphthalene derivatives of potential medicinal importance has been developed involving tandem applications of Claisen rearrangement and ring-closing diene metathesis as key steps. Copyright Taylor & Francis Group, LLC.
Diversity-oriented approach to biologically relevant molecular frameworks starting with β-naphthol and using the claisen rearrangement and olefin metathesis as key steps
A diversity-oriented approach for the synthesis of various structurally different molecular frameworks from readily accessible and common precursors is described. A Claisen rearrangement followed by ring-closing metathesis or ethylene-promoted ring-closin
Kotha, Sambasivarao,Mandai, Kalyaneswar,Tiwari, Arti,Mobin, Shaikh M.
p. 8024 - 8038
(2007/10/03)
THE CLAISEN REARRANGEMENT OF SOME ALLYL-β-NAPHTHYL ETHERS AND CYCLIZATION OF THE PRODUCTS
Some allyl-2-carboxy-3-hydroxy- as well as 2,3- and 2,7-diallyloxynaphtalenes were obtained.Respectively rearranged compounds were cyclized to naphthodihydrofuran rings.
Prajer-Janczewska, Lidia,Wroblewski, Juliusz
p. 1431 - 1437
(2007/10/02)
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