0000000001305061
AUTHOR
Wei Xia
Synthesis of Polycyclic Indolines by Utilizing a Reduction/Cyclization Cascade Reaction
European journal of organic chemistry 2021(45), 6097-6101 (2021). doi:10.1002/ejoc.202101191
Synthesis of N‐Fused Indolines via Copper (II)‐Catalyzed Dearomatizing Cyclization of Indoles
Advanced synthesis & catalysis 363(12), 3121-3126 (2021). doi:10.1002/adsc.202100290
Synthesis of Polycyclic Indolines utilizing a reduction/cyclization cascade reaction
Subsequent reduction and dearomatizing cyclization reactions open up an entry into the synthesis of novel N-fused polycyclic indolines. The dearomatizing cyclization as key step of the sequence proceeds well with Cu(OTf)2 or TfOH as catalyst. At elevated temperature reduction of nitro-substituted precursors with iron under acidic conditions affords a broad variety of polycyclic indolines directly in a two-step cascade reaction in good to excellent yields. Using the developed protocol, the alkaloids Tryptanthrin and Phaitanthrin C have been prepared. peerReviewed
Cover Feature: Synthesis of Polycyclic Indolines by Utilizing a Reduction/Cyclization Cascade Reaction (Eur. J. Org. Chem. 45/2021)
CCDC 2067949: Experimental Crystal Structure Determination
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CCDC 2067947: Experimental Crystal Structure Determination
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CCDC 2067946: Experimental Crystal Structure Determination
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CCDC 2067943: Experimental Crystal Structure Determination
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CCDC 2067948: Experimental Crystal Structure Determination
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CCDC 2080687: Experimental Crystal Structure Determination
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CCDC 2067945: Experimental Crystal Structure Determination
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CCDC 2080689: Experimental Crystal Structure Determination
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CCDC 2067944: Experimental Crystal Structure Determination
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CCDC 2080691: Experimental Crystal Structure Determination
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CCDC 2080688: Experimental Crystal Structure Determination
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CCDC 2080690: Experimental Crystal Structure Determination
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