Tandem SNAr/Aldol Condensation of Oxindoles with o-Haloacetophenones Enables Modular Assembly of 2,3-Fused Indolines Bearing a Quaternary Carbon DOI
Zhiping Zheng,

Kai-Heng Yu,

Ziyuan Liu

et al.

The Journal of Organic Chemistry, Journal Year: 2025, Volume and Issue: unknown

Published: April 28, 2025

Described herein is a novel base-promoted [4 + 2] annulation reaction of 3-methyl-indolin-2-ones with ortho-haloacetophenones, which enables the modular and reliable synthesis 2,3-fused indolines bearing quaternary carbon. Two C-C bonds can be successively constructed through tandem sequence involving SNAr aldol condensation. This protocol highlighted by transition metal-free conditions, high efficiency, simple operation.

Language: Английский

Tandem SNAr/Aldol Condensation of Oxindoles with o-Haloacetophenones Enables Modular Assembly of 2,3-Fused Indolines Bearing a Quaternary Carbon DOI
Zhiping Zheng,

Kai-Heng Yu,

Ziyuan Liu

et al.

The Journal of Organic Chemistry, Journal Year: 2025, Volume and Issue: unknown

Published: April 28, 2025

Described herein is a novel base-promoted [4 + 2] annulation reaction of 3-methyl-indolin-2-ones with ortho-haloacetophenones, which enables the modular and reliable synthesis 2,3-fused indolines bearing quaternary carbon. Two C-C bonds can be successively constructed through tandem sequence involving SNAr aldol condensation. This protocol highlighted by transition metal-free conditions, high efficiency, simple operation.

Language: Английский

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