Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5265208 | Tetrahedron Letters | 2012 | 5 Pages |
Abstract
A one-pot protocol toward several substituted 5,6-dihydrobenzo[4,5]imidazo[2,1-a]isoquinolines 1 starting with 2-allylbenzaldehydes 2 was described. The process was carried out the one-pot condensation/hydroamination reaction of substituted 2-allylbenzaldehydes 2 with 1,2-diaminobenzenes 3 in refluxing toluene in good yields. Skeleton 2 was prepared via one-pot ortho-metalative PhBCl2-mediated double alkylation of hydroxybenzaldehyde 4 with LDA in moderate yields.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Meng-Yang Chang, Ming-Hao Wu, Yeh-Long Chen,