Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/85864
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Type: Journal article
Title: An investigation of the reaction of dehydrogenating agents with a stable 8-Oxatricyclo[4,3,0,0⁷,⁹]nona-2,4-diene and related Bicylo[4,2,0]octa-2,4-dienes as a potential route to isobenzofurans
Other Titles: An investigation of the reaction of dehydrogenating agents with a stable 8-Oxatricyclo[4,3,0,0(7),(9)]nona-2,4-diene and related Bicylo[4,2,0]octa-2,4-dienes as a potential route to isobenzofurans
Author: Tan, R.Y.S.
Russell, R.A.
Warrener, R.N.
Citation: Australian Journal of Chemistry, 1981; 34(4):905-911
Publisher: CSIRO Publishing
Issue Date: 1981
ISSN: 0004-9425
1445-0038
Statement of
Responsibility: 
Richard Y. S. Tan, Richard A. Russell and, Ronald N. Warrener
Abstract: Reaction of the 7,8-dichlorobicyclo[4,2,0]octa-2,4-diene (9) with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone yields the benzocyclobutene (10). Extension of this technique to the related bicyclo[4,2,0]octa-2,4,7-trienes (21) and (23), or 8-oxatricyclo[4,3,0,07,9]nona-2,4-diene (6) was unsuccessful. Manganese dioxide was equally unrewarding while o-chloranil reacted with these olefins to yield benzodioxins in a [4+2] cycloaddition reaction.
Rights: © CSIRO 1981
RMID: 0030009260
DOI: 10.1071/CH9810905
Appears in Collections:Chemistry publications

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