科研速览 · Science Skim继续刷下去 · Keep skimming →
◆ Organic letters2026-09-11

Nickel-Catalyzed Regio- and Diastereoselective Ring-Opening Reductive Coupling of Methylenecyclopropanes with Aldehydes.

Min Ou, Zhi-Juan He, Long Tian, Zhicheng Yuan, Hongwei Chu, Yuanhong Ma

原始摘要(英文原文)· Original abstract
Transition-metal-catalyzed selective transformations of strained small ring systems are of great significance yet challenging. Herein, we disclose a nickel-catalyzed regio- and diastereoselective ring-opening reductive coupling of methylenecyclopropanes with aldehydes. The method offers an efficient route to bishomoallylic alcohols under mild conditions with a broad substrate scope (37 examples), good functional group tolerance, and generally high diastereoselectivity.
读原文 · Read the paper ↗

AI 追问PRO

登录后使用 AI 追问

讨论区

登录后参与讨论

相关论文 · Related

Nickel-Catalyzed Regio- and Diastereoselective Ring-Opening Reductive Coupling of Methylenecyclopropanes with Aldehydes. — 科研速览 Science Skim