Recent synthetic methodologies for imidazo[1,5-a]pyridines and related heterocycles

被引：26

作者：

Ramana Reddy, Mittapalli ^{[1
]}

Darapaneni, Chandra Mohan ^{[2
]}

Patil, Rajendra D. ^{[3
]}

Kumari, Harshita ^{[1
]}

机构：

[1] Univ Cincinnati, James L Winkle Coll Pharm, Cincinnati, OH 45267 USA

[2] Paraza Pharma Inc, Montreal, PQ H4S 2E1, Canada

[3] Moolji Jaitha Coll, Sch Chem Sci, Jalgaon 425001, Maharashtra, India

来源：

ORGANIC & BIOMOLECULAR CHEMISTRY | 2022年 / 20卷 / 17期

关键词：

CATALYZED DENITROGENATIVE TRANSANNULATION; AEROBIC OXIDATIVE AMINATION; ONE-POT SYNTHESIS; C-H AMINATION; C(SP(3))-H BONDS; EFFICIENT SYNTHESIS; CARBENE LIGANDS; HIGHLY POTENT; AMINO-ACIDS; CYCLIZATION;

D O I：

10.1039/d2ob00386d

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Imidazo[1,5-a]pyridine is a significant structural component of a large number of agrochemicals and pharmaceuticals. The synthesis of imidazo[1,5-a]pyridine has been a subject of intense research for numerous decades. A large number of transformations are now available to conveniently access imidazo[1,5-a]pyridine from readily available starting materials. This review details the recent development in imidazo[1,5-a]pyridine construction involving cyclocondensation, cycloaddition, oxidative cyclization, and transannulation reactions.

引用

页码：3440 / 3468

页数：29

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