Chemistry of O-arylhydroxylamines. A novel acid-catalyzed rearrangement of O-aryl-N-acetoacetylhydroxylamines to benzofurans
β Scribed by Yasuyuki Endo; Kohshi Namikawa; Koichi Shudo
- Publisher
- Elsevier Science
- Year
- 1986
- Tongue
- French
- Weight
- 209 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0040-4039
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A new rearrangement byproduct, 3-methyl-1,2,3,4,4a,4b,9a,15,15a,15b-decahydro-(4,5);(4a,15)-dimethanotricyclo-(4,3,1,0 2,7 )deca[8,9,1,10-a,b,c]pyrido[4,3-a]-acridin-6-en-9-ol-8-one, has been isolated from the acid-catalyzed O-demethylation of 7a-o-aminophenyl-6,14-endo-ethenotetrahydrothebaine. The
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