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The synthesis of 9,10-dimethoxy-2-methyl-1,4-anthraquinone, an unusual quinone, is achieved in 5 steps from p-benzoquinone. A Kochi-Anderson radical methylation features as a key step in the synthesis. The chemistry of a cyclopropa-1,4-anthracenedione is also described.

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Title The synthesis of 9,10-dimethoxy-2-methyl-1,4-anthraquinone, an unusual quinone, is achieved in 5 steps from p-benzoquinone. A Kochi-Anderson radical methylation features as a key step in the synthesis. The chemistry of a cyclopropa-1,4-anthracenedione is also described.
 
Creator RAY, SUTAPA
 
Subject Chemistry
Organic
 
Date 2008-09-03
 
Type Thesis
NonPeerReviewed
 
Format application/msword
 
Identifier http://eprints.csirexplorations.com/114/1/Abstract.doc
RAY, SUTAPA (2008) The synthesis of 9,10-dimethoxy-2-methyl-1,4-anthraquinone, an unusual quinone, is achieved in 5 steps from p-benzoquinone. A Kochi-Anderson radical methylation features as a key step in the synthesis. The chemistry of a cyclopropa-1,4-anthracenedione is also described. PhD thesis, INDIAN INSTITUTE OF TECHNOLOGY, KHARAGPUR.
 
Relation http://eprints.csirexplorations.com/114/