Convergent Assembly of 1,4-Benzothiazide Spiroindolinones via [4 + 2] Spiroannulation Under Open-Air Conditions DOI
Wenxiang Hu,

Kai-Heng Yu,

Feng‐Cheng Jia

и другие.

The Journal of Organic Chemistry, Год журнала: 2024, Номер 89(22), С. 16531 - 16541

Опубликована: Ноя. 4, 2024

This report discloses a transition-metal-free [4 + 2] spirocyclization of isatin-derived β-silylcarbinols and 2-aminobenzenethiols, providing facile approach to 1,4-benzothiazide spiroindolinones in decent yields. Control experiments indicate that 3-methylene oxindoles disulfides are key intermediates this tandem reaction. Moreover, the resulting products can be facilely converted into pharmaceutically significant sulfone sulfoxide scaffolds, which further demonstrates potential utility protocol.

Язык: Английский

Convergent Assembly of 1,4-Benzothiazide Spiroindolinones via [4 + 2] Spiroannulation Under Open-Air Conditions DOI
Wenxiang Hu,

Kai-Heng Yu,

Feng‐Cheng Jia

и другие.

The Journal of Organic Chemistry, Год журнала: 2024, Номер 89(22), С. 16531 - 16541

Опубликована: Ноя. 4, 2024

This report discloses a transition-metal-free [4 + 2] spirocyclization of isatin-derived β-silylcarbinols and 2-aminobenzenethiols, providing facile approach to 1,4-benzothiazide spiroindolinones in decent yields. Control experiments indicate that 3-methylene oxindoles disulfides are key intermediates this tandem reaction. Moreover, the resulting products can be facilely converted into pharmaceutically significant sulfone sulfoxide scaffolds, which further demonstrates potential utility protocol.

Язык: Английский

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