Canadian Journal of Chemistry

The bromination-methanolysis of N-acetyl-2, 3-dimethylindole

SF Vice, GI Dmitrienko

Index: Vice, Susan F.; Dmitrienko, Gary I. Canadian Journal of Chemistry, 1982 , vol. 60, p. 1233 - 1237

Full Text: HTML

Citation Number: 6

Abstract

Bromination of N-acetyl-2, 3-dimethylindole 11 in the presence of excess methanol at room temperature gave a mixture of products consisting of cis and trans N-acetyl-2, 3-dimethoxy- 2, 3-dimethylindoline 17 and 18, 3-methoxy-2, 3-dimethylindolenine 19, and N-acetyl-3- methoxymethyl-2-methylindole 21. The same reaction performed at-40° C yielded a mixture of 17, 18, and N-acetyl-2-methoxy-2-methyl-3-methyleneindoline 22. Bromination of 11 at ...

Related Articles:

C-2 side chain alkylation of 2-methyl-3-alkylindoles via 3-methoxyindolenines

[Vice, Susan F.; Gross, Edward A.; Friesen, Richard W.; Dmitrienko, Gary I. Tetrahedron Letters, 1982 , vol. 23, # 8 p. 829 - 832]

The bromination and chlorination of 2, 3-dialkylindoles. Isolation of 3-bromo-and 3-chloro-2, 3-dialkylindolenines and acid catalyzed conversion to 3- …

[Dmitrienko, Gary I.; Gross, Edward A.; Vice, Susan F. Canadian Journal of Chemistry, 1980 , vol. 58, p. 808 - 814]

Alkoxylation of 2, 3-dialkylindoles utilizing iodosobenzene diacetate

[Awang, Dennis V. C.; Vincent, Andre Canadian Journal of Chemistry, 1980 , vol. 58, # 15 p. 1589 - 1591]

More Articles...