Benzo[7,8]indolizinoquinoline scaffolds based on Mg(ClO4)2-promoted regiospecific imide reduction and π-cyclization of N-acyliminium species. Analogues of the topo-1 poison rosettacin and 22-hydroxyacuminatine alkaloids-Reference-Cited by-同舟云学术

Benzo[7,8]indolizinoquinoline scaffolds based on Mg(ClO4)2-promoted regiospecific imide reduction and π-cyclization of N-acyliminium species. Analogues of the topo-1 poison rosettacin and 22-hydroxyacuminatine alkaloids

Published:2019-07 Issue:5 Volume:12 Page:680-693
ISSN:1878-5352
Container-title:Arabian Journal of Chemistry
language:en
Short-container-title:Arabian Journal of Chemistry

Author:

Hamid Abdulkareem,Souizi Abdelaziz,Lawson Ata Martin,Othman Mohamed,Ghinet Alina,Rigo Benoît,Daïch Adam

Publisher

Elsevier BV

Subject

General Chemical Engineering,General Chemistry

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3. Toward new camptothecins. Part 5: On the synthesis of precursors for the crucial Friedländer reaction

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5. Studies on pyrrolidinones. Oxidations and rearrangements in the hexahydrobenz[f]indolizine-3,10-dione series

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