Journal
ASIAN JOURNAL OF ORGANIC CHEMISTRY
Volume 11, Issue 3, Pages -Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/ajoc.202100798
Keywords
C-H activation; 1; 8-naphthalimide; Regioselectivity; Alkenylation
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Funding
- DST-SERB, New Delhi [CRG/2018/002159]
- CSIR, New Delhi [02(0310)/17/EMR-II]
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In this study, direct C-H alkenylation of 1,8-naphthalimide using cyclic imide as a weak directing group and ruthenium catalyst was explored. The alkenyl group(s) were successfully introduced into the 1,8-naphthalimide skeleton at the inactive C2 and/or C7 positions. The aromatic ring of 1,8-naphthalimide was substituted with electron-withdrawing and electron-donating groups, and N-alkyl/aryl groups on cyclic imide were found compatible in these coupling reactions.
Ruthenium-catalyzed direct C-H alkenylation of 1,8-naphthalimide has been explored using cyclic imide as a weak directing group and successfully introduce alkenyl group(s) into 1,8-naphthalimide skeleton at the inactive C2 and/or C7 position(s). The aromatic ring of 1,8-naphthalimide is substituted with electron-withdrawing and -donating groups, and N-alkyl/aryl groups on cyclic imide are compatible in these coupling reactions.
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