oxepins and 2-naphthol

oxepins has been researched along with 2-naphthol* in 1 studies

Other Studies

1 other study(ies) available for oxepins and 2-naphthol

Article	Year
Diversity-oriented approach to biologically relevant molecular frameworks starting with beta-naphthol and using the Claisen rearrangement and olefin metathesis as key steps. Chemistry (Weinheim an der Bergstrasse, Germany), 2006, Oct-25, Volume: 12, Issue:31 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-closing enyne metathesis has been utilized as the key synthetic transformation to generate naphthoxepine derivatives. The ring-closing metathesis approach has also been used to generate spirocyclic compounds and the pleiadene framework. Topics: Alkenes; Combinatorial Chemistry Techniques; Naphthols; Oxepins	2006

Article

Year

Diversity-oriented approach to biologically relevant molecular frameworks starting with beta-naphthol and using the Claisen rearrangement and olefin metathesis as key steps.

Chemistry (Weinheim an der Bergstrasse, Germany), 2006, Oct-25, Volume: 12, Issue:31

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-closing enyne metathesis has been utilized as the key synthetic transformation to generate naphthoxepine derivatives. The ring-closing metathesis approach has also been used to generate spirocyclic compounds and the pleiadene framework.

Topics: Alkenes; Combinatorial Chemistry Techniques; Naphthols; Oxepins

2006