Efficient synthesis of functionalized 1, 3-dihydroisobenzofurans from salicylaldehydes: Application to the synthesis of escitalopram
P Wang, R Zhang, J Cai, JQ Chen, M Ji
Index: Wang, Peng; Zhang, Rui; Cai, Jin; Chen, Jun-Qing; Ji, Min Chinese Chemical Letters, 2014 , vol. 25, # 4 p. 549 - 552
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Citation Number: 3
Abstract
Abstract An efficient synthesis of substituted 1, 3-dihydroisobenzofurans is developed. In this novel route, o-aroylbenzaldehydes, as key intermediates, can be obtained by lead tetraacetate oxidation of N-aroylhydrazones of salicylaldehydes. The mild and general strategy enables the synthesis of various substituted 1, 3-dihydroisobenzofurans in high yields. Moreover, this method can be applied to efficiently synthesize escitalopram.
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