4.4 Article

Novel synthesis of tetrahydro-1H-pyrrolo[1,2-a]imidazol-2-ones via decarboxylative cyclization reaction of α-amino acids and α-ketoamides

期刊

TETRAHEDRON LETTERS
卷 58, 期 6, 页码 546-551

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2016.12.079

关键词

alpha-Ketoamide; alpha-Amino acid; Azomethine ylide; Decarboxylative cyclization; Tetrahydro-1H-pyrrolo[1,2-a]imidazol-2-ones

资金

  1. Natural Science Foundation of China [21402137, 21302135]
  2. Chemical Engineering & Technology of Zhejiang Province First-Class Discipline (Taizhou University)

向作者/读者索取更多资源

An efficient and practical method was developed for the synthesis of tetrahydro-1H-pyrrolo[1,2-a]imidazol-2-ones based on the decarboxylative cyclization reaction of alpha-ketoamides and proline. In most cases,tetrahydro-1H-pyrrolo[1,2-a]imidazol-2-ones were obtained with perfect diastereoselectivity to give trans-isomer in excellent yield. (C) 2016 Elsevier Ltd. All rights reserved.

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