Sequential decarboxylative azide-alkyne cycloaddition and dehydrogenative coupling reactions: one-pot synthesis of polycyclic fused triazoles

被引:7
|
作者
Bharathimohan, Kuppusamy [1 ,2 ]
Ponpandian, Thanasekaran [3 ]
Ahamed, A. Jafar [1 ]
Bhuvanesh, Nattamai [4 ]
机构
[1] Bharathidasan Univ, Jamal Mohamed Coll, PG & Res Dept Chem, Thiruchirapalli 620020, Tamil Nadu, India
[2] Orchid Chem & Pharmaceut Ltd, R&D Ctr, Drug Discovery Res, Madras 600119, Tamil Nadu, India
[3] Inogent Labs Pvt Ltd, API R&D, IDA, Hyderabad 500076, Andhra Pradesh, India
[4] Texas A&M Univ, Dept Chem, Xray Diffract Lab, College Stn, TX 77842 USA
来源
关键词
copper(II) acetate; decarboxylative CuAAC; dehydrogenative coupling; fused triazoles; one-pot synthesis; H BOND FUNCTIONALIZATION; DIRECT ARYLATIONS; PALLADIUM; 1,2,3-TRIAZOLES; ACID; ACTIVATION; THIAZOLES; MECHANISM; INDOLES;
D O I
10.3762/bjoc.10.321
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Herein, we describe a one-pot protocol for the synthesis of a novel series of polycyclic triazole derivatives. Transition metal-catalyzed decarboxylative CuAAC and dehydrogenative cross coupling reactions are combined in a single flask and achieved good yields of the respective triazoles (up to 97% yield). This methodology is more convenient to produce the complex polycyclic molecules in a simple way.
引用
收藏
页码:3031 / 3037
页数:7
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