Hydride Transfer Involved Redox-Neutral Cascade Cyclizations for Construction of Spirocyclic Bisoxindoles Featuring a [3,4]-Fused Oxindole Moiety

The hydride transfer involved redox-neutral cascade cyclization has been developed to construct the spirocyclic bisoxindoles featuring a [3,4]-fused oxindole moiety from rationally designed C4-amine-substituted isatins, affording the diverse tricyclic [3,4]-fused oxindoles with three consecutive chi...

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Veröffentlicht in:Organic letters 2019-02, Vol.21 (4), p.1058-1062
Hauptverfasser: Li, Shuai-Shuai, Zhu, Shuai, Chen, Chunqi, Duan, Kang, Liu, Qing, Xiao, Jian
Format: Artikel
Sprache:eng
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Zusammenfassung:The hydride transfer involved redox-neutral cascade cyclization has been developed to construct the spirocyclic bisoxindoles featuring a [3,4]-fused oxindole moiety from rationally designed C4-amine-substituted isatins, affording the diverse tricyclic [3,4]-fused oxindoles with three consecutive chiral centers in good yields and excellent diastereoselectivities (>20:1).
ISSN:1523-7060
1523-7052
DOI:10.1021/acs.orglett.8b04100