Regiospecific C-9 substitution of ellipticine derivatives
A Langendoen, JPM Plug, GJ Koomen, UK Pandit
Index: Langendoen, Albert; Koomen, Gerrit-Jan; Pandit, Upendra K. Heterocycles, 1987 , vol. 26, # 1 p. 91 - 94
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Citation Number: 13
Abstract
6-Methylellipticine (6) undergoes acylation at the C (9)-position, under Friedel Crafts reaction conditions. The C (9)-formyl compound (8) rearranges to the corresponding hydroxy derivative (9) upon treatment with hydrogen peroxide, in methanol, in the presence of
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Regiospecific C-9 substitution of ellipticine derivatives
[Langendoen, Albert; Plug, Johannes P. M.; Koomen, Gerrit-Jan; Pandit, Upendra K. Tetrahedron, 1989 , vol. 45, # 6 p. 1759 - 1762]
Regiospecific C-9 substitution of ellipticine derivatives
[Langendoen, Albert; Plug, Johannes P. M.; Koomen, Gerrit-Jan; Pandit, Upendra K. Tetrahedron, 1989 , vol. 45, # 6 p. 1759 - 1762]