Photochemical Synthesis of Indolocarbazoles through Tandem Indolization/Dimerization/Mannich Cyclization from Allenes

Indolocarbazole alkaloids and their derivatives were discovered to have potent protein kinase and topoisomerase I inhibitory activities. Disclosed herein is the photochemical synthesis of the indolocarbazole ring system from N-allenyl-2-iodoanilines. The tandem protocol included visible-light-mediat...

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Veröffentlicht in:Organic letters 2022-05, Vol.24 (19), p.3582-3587
Hauptverfasser: Tang, Jiaying, Ren, Linlin, Li, Jianwei, Wang, Yonggong, Hu, Dongyan, Tong, Xiaogang, Xia, Chengfeng
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Sprache:eng
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Zusammenfassung:Indolocarbazole alkaloids and their derivatives were discovered to have potent protein kinase and topoisomerase I inhibitory activities. Disclosed herein is the photochemical synthesis of the indolocarbazole ring system from N-allenyl-2-iodoanilines. The tandem protocol included visible-light-mediated 5-exo-trig radical cyclization and subsequent radical dimerization, followed by acid-promoted deprotection and intramolecular Mannich cyclization. This strategy showed exceptional functional group tolerance and was successfully applied in the concise synthesis of natural products tjipanazoles B and D.
ISSN:1523-7060
1523-7052
DOI:10.1021/acs.orglett.2c01371