Selective Synthesis of 3-(1H-Tetrazol-5-yl)-indoles from 2H-Azirines and Arynes DOI Creative Commons
Carla Grosso, Cláudia Alves, Terver John Sase

и другие.

ACS Omega, Год журнала: 2024, Номер 9(27), С. 29282 - 29289

Опубликована: Июнь 24, 2024

A new selective synthetic approach to indole derivatives bearing a tetrazole moiety has been developed. Arynes, generated in situ from o-(trimethylsilyl)aryl triflates and KF, reacted smoothly with 2-(2-benzyl-2H-tetrazol-5-yl)-2H-azirines give 3-(2-benzyl-2H-tetrazol-5-yl)-indole high selectivity. Deprotection of the gave 3-(1H-tetrazol-5-yl)-indole derivatives.

Язык: Английский

2H‐Azirines: Recent Progress in Synthesis and Applications DOI
Fen Xu,

Fan‐Wang Zeng,

Wenjie Luo

и другие.

European Journal of Organic Chemistry, Год журнала: 2024, Номер 27(11)

Опубликована: Янв. 29, 2024

Abstract 2H ‐arizines are important three‐membered heterocycles in organic chemistry. Recently, many advances the synthesis and functionalization of have been reported. Neber rearrangement, isomerization isoxazole, oxidation enamine, C−H bond activation, decomposition vinyl azide, alkyne, multi‐step developed for efficient assembly ‐azirines. As versatile highly strained unsaturated heterocycles, ‐azirines can be used as distinctive building blocks towards significant functional groups, attracted extensive attention fabrication numerous heterocycles. Recent studies focused on [3+n] ring‐expansion reactions, nucleophilic addition C=N double or continuous followed by cyclization, ring‐opening to acyclic compounds, substitution sp 3 ‐C−H One most critical challenges is seeking a selective opening specific three bonds azirine circle, some what achieved basis metal catalyst, photocatalysis, combination catalyst photocatalysis. In this review, recent involving reactivity accompanied with breakthroughs summarized. The review mainly covers period from 2019 2023.

Язык: Английский

Процитировано

12

Selective Synthesis of 3-(1H-Tetrazol-5-yl)-indoles from 2H-Azirines and Arynes DOI Creative Commons
Carla Grosso, Cláudia Alves, Terver John Sase

и другие.

ACS Omega, Год журнала: 2024, Номер 9(27), С. 29282 - 29289

Опубликована: Июнь 24, 2024

A new selective synthetic approach to indole derivatives bearing a tetrazole moiety has been developed. Arynes, generated in situ from o-(trimethylsilyl)aryl triflates and KF, reacted smoothly with 2-(2-benzyl-2H-tetrazol-5-yl)-2H-azirines give 3-(2-benzyl-2H-tetrazol-5-yl)-indole high selectivity. Deprotection of the gave 3-(1H-tetrazol-5-yl)-indole derivatives.

Язык: Английский

Процитировано

0