Transition metal-free Suzuki type cross-coupling reaction for the synthesis of dissymmetric ketones

被引:4
|
作者
Jadhav, Sanjay [1 ]
Rashinkar, Gajanan [1 ]
Salunkhe, Rajashri [1 ]
Kumbhar, Arjun [2 ]
机构
[1] Shivaji Univ, Dept Chem, Kolhapur 416004, MS, India
[2] PDVP Coll, Dept Chem, Sangli 416312, MS, India
关键词
Metal-free coupling; Base; Dissymmetric ketones; Suzuki reaction; FRIEDEL-CRAFTS ACYLATION; PALLADIUM-CATALYZED SYNTHESIS; ARYLBORONIC ACIDS; BORONIC ACIDS; ARYL KETONES; CARBOXYLIC-ACIDS; IONIC LIQUIDS; HALIDES; PROTODEBORONATION; SUBSTITUTION;
D O I
10.1016/j.tetlet.2017.06.048
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A simple, efficient and metal-free route for the synthesis of dissymmetric ketones through Suzuki type cross-coupling reaction has been established. This strategy signifies an attractive, cost-effective and operationally convenient tool for the synthesis of a wide range of dissymmetric ketones. Although conventional routes for the synthesis of ketones have been widely used, the potential challenge with these methods is functional group tolerance. The reported metal-free method represents a reaction with moderate functional group tolerance. The procedure is operationally convenient and shows broad substrate scope with good to excellent product yields. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3201 / 3204
页数:4
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