Nickel-catalyzed esterification of mandelic acids with alcohols

被引:4
|
作者
Liu, Changhong
Marhaba, Mamat
Dilshat, Abdukerem
Zhu, Wenli
Xia, Kun
Mao, Zechuan
Ablimit, Abdukader [1 ]
机构
[1] State Key Lab Chem & Utilizat Carbon Based Energy, Urumqi 830017, Xinjiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Mandelate; Nickel(II)-catalyzed; Esterification; Alcohols; FRIEDEL-CRAFTS REACTION; ALPHA-OXYACYLATION; CARBONYL-COMPOUNDS; CARBOXYLIC-ACIDS; BORIC-ACID; ACYLOXYLATION; CYCLANDELATE; DERIVATIVES; INDOLES; KETONES;
D O I
10.1016/j.arabjc.2022.104407
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Mandelates and their derivatives are widely used in organic synthesis, drug discovery, biodegradable polymers and other related fields. Therefore, the effective and simple synthesis of these compounds has attracted much attention. In this paper, a nickel(II)-catalyzed esterification of mandelic acids with different alcohols was realized for the synthesis of mandelic acid esters. This transformation was conducted under mild reaction conditions with yields up to 95%, and was suc-cessfully utilized in the gram-scale synthesis of medicine cyclandelate.(c) 2022 The Author(s). Published by Elsevier B.V. on behalf of King Saud University.This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页数:8
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