Title: SYNTHETIC STUDIES TOWARDS FAVELINE METHYL-ETHER
Authors: HO, TL
CHEN, CK
應用化學系
Department of Applied Chemistry
Issue Date: 15-May-1995
Abstract: A convergent approach to faveline methyl ether based on Claisen rearrangement is delineated Thus the benzylic and allylic alcohol substrate was assembled by a Grignard reaction, and the rearrangement product was oxidized and cyclized. Double bond isomers of faveline methyl ether were obtained.
URI: http://dx.doi.org/10.1016/0040-4020(95)00240-9
http://hdl.handle.net/11536/1917
ISSN: 0040-4020
DOI: 10.1016/0040-4020(95)00240-9
Journal: TETRAHEDRON
Volume: 51
Issue: 20
Begin Page: 5819
End Page: 5824
Appears in Collections:Articles


Files in This Item:

  1. A1995QY11200010.pdf

If it is a zip file, please download the file and unzip it, then open index.html in a browser to view the full text content.