4.4 Article

Selective reduction of aromatic azides in solution/solid-phase and resin cleavage by employing BF3•OEt2/EtSH.: Preparation of DC-81

期刊

TETRAHEDRON LETTERS
卷 47, 期 25, 页码 4253-4257

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PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2006.04.025

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pyrrolo[2,1-c][1,4]benzodiazepines; solid-phase synthesis; boron trifluoride diethyletherate; resin cleavage; reductive cyclization

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An efficient method for the reduction of aromatic azides in both solution and solid-phase has been developed by employing (BF3OEt2)-O-./EtSH. This report also describes resin cleavage employing this reagent system. Further, this protocol has been utilized for the solution as well as the solid-phase synthesis of pyrrolo[2, 1-c][1,4]benzodiazepines, including the naturally occurring antibiotic DC-81 and fused [2,1-b]quinazolinones. (c) 2006 Elsevier Ltd. All rights reserved.

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