Strategies for the organocatalytic asymmetric synthesis of bridged acetal

被引：1

作者：

Balha, Megha ^{[1
]}

Vagadiya, Nikunjkumar ^{[1
]}

Manhas, Anu ^{[1
]}

机构：

[1] Pandit Deendayal Energy Univ, Dept Chem, Gandhinagar 382426, Gujarat, India

来源：

MATERIALS TODAY-PROCEEDINGS | 2022年 / 62卷 / P13期

关键词：

Asymmetric; Organocatalysts; Bridged acetal; Chiral; Methanobenzodioxepine; ENANTIOSELECTIVE SYNTHESIS; NATURAL-PRODUCTS; DIRECT ACCESS; ANTIPLATELET; SPIROACETALS; SPIROKETALS; PALLADIUM; CATALYSIS; GOLD;

D O I：

10.1016/j.matpr.2021.12.546

中图分类号：

T [工业技术];

学科分类号：

08 ;

摘要：

Most of the natural products and biologically active molecules have acetals as their building block. As per the research, the biological activity of the chiral acetals is superior to their racemates. Owing to the racemization, the asymmetric synthesis of chiral acetal is challenging, and thus it attracts the research community's interest. In the present review, various strategies devised for the synthesis of chiral O,O- acetals having spirooxindoles scaffold have been discussed. Copyright (c) 2021 Elsevier Ltd. All rights reserved. Selection and peer-review under responsibility of the scientific committee of the International Conference Additive Manufacturing and Advanced Materials-AM2 2021.

引用

页码：7007 / 7018

页数：12

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