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