Simple jQuery Dropdowns
Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/23164
Title: Two protocols for the conversion of biphenol to binaphthol: Synthesis of diospyrol
Authors: Nopporn Thasana
Somchai Pisutjaroenpong
Somsak Ruchirawat
Chulabhorn Research Institute
The Institute of Science and Technology for Research and Development, Mahidol University
Keywords: Chemistry
Issue Date: 3-May-2006
Citation: Synlett. No.7 (2006), 1080-1084
Abstract: The application of directed orthometallation (DoM), Fries rearrangement and transmetallation followed by allylation and cyclization is reported for the conversion of biphenol to binaphthol as a means for the synthesis of diospyrol. Furthermore, the same transformation can be accomplished by the reaction of the dienolate anion of an α,β-unsaturated amide with an aryne intermediate. © Georg Thieme Verlag Stuttgart.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33646548606&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/23164
ISSN: 09365214
Appears in Collections:Scopus 2006-2010

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.