期刊
HETEROCYCLES
卷 82, 期 2, 页码 1297-+出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.3987/COM-10-S(E)77
关键词
Flow Chemistry; Micro-Reactor; Cycloaddition; Pyrrolidine; Heterocycle
资金
- Cambridge European Trust
- Ralph Raphael Studentship
- Royal Society
- Fonds der Chemischen Industrie
- BP1702
We expand upon recent results concerning dipolar cycloaddition reactions of unstabilized azomethine ylids with nitro alkenes to generate 3-nitropyrrolidines via a flow chemistry sequence. This new work describes the development of a three-component coupling reaction between glycine esters, aldehydes and nitro alkenes. In order to further demonstrate the utility of flow technology in concert with heterogeneous reagents and scavengers for complex reaction sequences an in-line oxidation resulting in the conversion of tetra-substituted pyrrolidines to their pyrrole congeners has been developed.
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