Journal
HETEROCYCLES
Volume 82, Issue 2, Pages 1297-+Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.3987/COM-10-S(E)77
Keywords
Flow Chemistry; Micro-Reactor; Cycloaddition; Pyrrolidine; Heterocycle
Categories
Funding
- Cambridge European Trust
- Ralph Raphael Studentship
- Royal Society
- Fonds der Chemischen Industrie
- BP1702
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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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