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.
Open Access Repository of Indian Theses: CSIR
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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.
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Creator |
RAY, SUTAPA
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Subject |
Chemistry
Organic |
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Date |
2008-09-03
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Type |
Thesis
NonPeerReviewed |
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Format |
application/msword
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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. |
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Relation |
http://eprints.csirexplorations.com/114/
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