| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5271223 | Tetrahedron Letters | 2013 | 4 Pages |
Abstract
An efficient protocol to generate indolo[1,2-c]quinazolines from acyclic alkyne substrates by ZnBr2-promoted domino hydroamination-cyclization has been established. The dichotomous properties of zinc salts involving alkynophilicity and oxophilicity assure a one-pot formation of five- and six-membered nitrogen-containing rings in the skeleton.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
![Assembly of indolo[1,2-c]quinazolines using ZnBr2-promoted domino hydroamination-cyclization](/preview/png/5271223.png "First Page Preview: Assembly of indolo[1,2-c]quinazolines using ZnBr2-promoted domino hydroamination-cyclization")
Authors
Min Xu, Ke Xu, Shaozhong Wang, Zhu-Jun Yao,