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◆ The Journal of Organic Chemistry2026-02-11· Chemoselectivity

Sequential [3 + 2] Annulation/Intramolecular Transesterification of <i>o</i> -Hydroxyaryl Azomethines and Conjugated Dienes: Access to Chromeno[4,3- <i>b</i> ]pyrrolidines

Zhenjie Gan, Ganyi Fan, Jiachen Jiang, Yue Wang, Er-Qing Li

原始摘要(英文原文)· Original abstract
Herein, we report a domino cyclization reaction of o -hydroxyaryl azomethines with electron-deficient conjugated dienes. This method provides a novel and efficient pathway for the construction of chromeno[4,3- b ]pyrrolidine derivatives. The protocol exhibits excellent chemoselectivity and a broad substrate scope. Furthermore, the reaction can be scaled up to gram quantities under the standard conditions.
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Sequential [3 + 2] Annulation/Intramolecular Transesterification of <i>o</i> -Hydroxyaryl Azomethines and Conjugated Dienes: Access to Chromeno[4,3- <i>b</i> ]pyrrolidines — 科研速览 Science Skim