4.4 Article

Synthesis of pyrrolo[1,3]diazepines by a dipolar cycloaddition-retro-Mannich domino reaction

Journal

TETRAHEDRON LETTERS
Volume 50, Issue 49, Pages 6810-6813

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2009.09.107

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Funding

  1. NIH [P50-GM067082]

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Microwave irradiation facilitated the synthesis of 4-arylthio-3-oxazolin-5-ones front ethyl cyanoformate, thiophenol, and cyclic ketones. Subsequent decarboxylation and in Situ [3+2] cycloaddition provided novel 2,3,4,5-tetrahydro-1H-pyrrolo[1,2-c][1,3]diazepine scaffolds after a spontaneous retro-Mannich domino reaction. (C) 2009 Elsevier Ltd. All rights reserved.

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