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

Published on 2019-02-12T16:25:32Z (GMT) by
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).

Cite this collection

Li, Shuai-Shuai; Zhu, Shuai; Chen, Chunqi; Duan, Kang; Liu, Qing; Xiao, Jian (2019): Hydride Transfer Involved Redox-Neutral Cascade Cyclizations

for Construction of Spirocyclic Bisoxindoles Featuring a [3,4]-Fused

Oxindole Moiety. ACS Publications. Collection.