期刊
ORGANIC LETTERS
卷 20, 期 3, 页码 602-604出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.7b03721
关键词
-
资金
- NIH-NIGMS [R01GM101389]
- UGC, New Delhi
Indolizidine and quinolizidine derivatives are readily assembled from L-proline or (+/-)-pipecolic acid and beta-ketoaldehydes via a decarboxylative annulation process. These reactions are promoted by acetic acid and involve azomethine ylides as reactive intermediates.
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