4.4 Article

Sequential decarboxylative [3+2] cycloaddition and Staudinger/aza-Wittig reactions for diastereoselective synthesis of tetrahydro-pyrroloquinazolines and tetrahedro-pyrrolobenzodiazepines

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TETRAHEDRON LETTERS
卷 61, 期 2, 页码 -

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PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2019.151392

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[3+2] cycloaddition; Decarboxylative; Aza-Wittig reaction; Tetrahydro-pyrroloquinazolines

资金

  1. Jiangsu oversea Visiting Scholar Program for University Prominent Youth & Middle-aged Teachers and Presidents

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A method for diastereoselective synthesis of tetrahydro-pyrroloquinazolines and tetrahydro-pyrrolobenzodiazepines is developed through sequential reactions including decarboxylative 1,3-dipolar cycloaddition of non-stabilized azomethine ylides, N-acylation or N-alkylation, and the Staudinger/aza-Wittig reactions. (C) 2019 Published by Elsevier Ltd.

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