期刊
ORGANIC LETTERS
卷 4, 期 9, 页码 1471-1474出版社
AMER CHEMICAL SOC
DOI: 10.1021/ol025659j
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资金
- NIGMS NIH HHS [GM55382] Funding Source: Medline
[GRAPHIC] The cyclization of aminoalkenes bearing an electron-withdrawing group on the nitrogen atom was catalyzed by triflic or sulfuric acid in toluene. Pyrrolidines and piperidines were formed in excellent yields. N-Phenylanilides also underwent cyclization to form gamma-lactams.
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