Towards click chemistry: Multicomponent reactions via combinations of name reactions

被引：50

作者：

Heravi, Majid M. ^{[1
]}

Zadsirjan, Vahideh ^{[1
]}

Dehghani, Mahzad ^{[1
]}

Ahmadi, Tahereh ^{[1
]}

机构：

[1] Alzahra Univ, Sch Sci, Dept Chem, Tehran, Iran

来源：

TETRAHEDRON | 2018年 / 74卷 / 27期

基金：

美国国家科学基金会;

关键词：

Multicomponent reaction; Click chemistry; Name reaction; Heterocycles; Knoevenagel reaction; Michael reaction; Diels-Alder reaction; Aldol reaction; Mannich reaction; Ugi reaction; Heck reaction; Huisgen reaction; Suzuki reaction; ONE-POT SYNTHESIS; KNOEVENAGEL-MICHAEL REACTION; MODIFIED POLY(STYRENE-CO-MALEIC ANHYDRIDE); PALLADIUM-CATALYZED VINYLATION; DIELS-ALDER REACTIONS; HUISGEN 1,3-DIPOLAR CYCLOADDITION; ASYMMETRIC ALDOL REACTIONS; REGIOSELECTIVE SYNTHESIS; EFFICIENT SYNTHESIS; RECYCLABLE CATALYST;

D O I：

10.1016/j.tet.2018.04.076

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

In this report, we try to show the importance of incorporation of name reactions in the sequential cascade reaction in which significantly decreasing the number of steps towards an ideal and practical multi-step synthesis of natural products as well showing virtually all the advantages already mentioned for "Click Chemistry". In addition, since the chiral inductions are desired for most of these sequential name reactions, their asymmetric catalyzed reactions were also described. (C) 2018 Elsevier Ltd. All rights reserved.

引用

页码：3391 / 3457

页数：67

共 278 条

[81] In situ prepared CuI nanoparticles on modified poly(styrene-co-maleic anhydride): an efficient and recyclable catalyst for the azide-alkyne click reaction in water [J].