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连续脱羧叠氮-炔环加成和脱氢偶联反应:多环稠合三唑的一锅合成。

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

机构信息

PG and Research Department of Chemistry, Jamal Mohamed College, affiliated to the Bharathidasan university, Thiruchirapalli - 620020, Tamilnadu, India ; Orchid Chemicals & Pharmaceuticals Ltd, Drug Discovery Research, R&D Center, Sholinganallur, Chennai - 600119, India.

Inogent Laboratories Pvt Ltd, API R&D, 28A, IDA, Nacharam, Hyderabad-500076, India.

出版信息

Beilstein J Org Chem. 2014 Dec 17;10:3031-7. doi: 10.3762/bjoc.10.321. eCollection 2014.

Abstract

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.

摘要

在这里,我们描述了一种一锅法合成新型多环三唑衍生物的方法。在单个烧瓶中结合了过渡金属催化的脱羧 CuAAC 和脱氢交叉偶联反应,以获得相应三唑的良好产率(高达 97%的产率)。这种方法更方便以简单的方式生产复杂的多环分子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ccac/4311670/06d0276f40e6/Beilstein_J_Org_Chem-10-3031-g003.jpg

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