期刊
SYNTHESIS-STUTTGART
卷 -, 期 23, 页码 4007-4014出版社
GEORG THIEME VERLAG KG
DOI: 10.1055/s-0030-1258266
关键词
N-ylides; indolizine polycycles; 1,3-dipolar cycloadditions; one-pot reaction; electron-deficient alkenes
资金
- Jiangsu Key Laboratory for Chemistry of Low-Dimensional Materials [JSKC09067]
- Huaiyin Normal University
3-Arylindolizines were prepared by one-pot domino reactions from benzyl halides with pyridine (or isoquinoline) and cyclic or acyclic dihalide-substituted electron-deficient alkenes in the presence of potassium carbonate via in situ generated N-ylide intermediate. Both electron-donating and electron-withdrawing groups are tolerated in the aryl ring of benzyl halides. The yields range from moderate to high.
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