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pubmed-article:17867694pubmed:abstractTextA mild, photoactivated 1,3-dipolar cycloaddition procedure was successfully developed for the synthesis of polysubstituted pyrazolines. This procedure involved the in situ generation of the reactive nitrile imine dipoles using a hand-held UV lamp at 302 nm, followed by spontaneous cycloaddition with a broad range of 1,3-dipolarophiles with excellent solvent compatibility, functional group tolerance, regioselectivity, and yield.lld:pubmed
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pubmed-article:17867694pubmed:articleTitleConvenient synthesis of highly functionalized pyrazolines via mild, photoactivated 1,3-dipolar cycloaddition.lld:pubmed
pubmed-article:17867694pubmed:affiliationDepartment of Chemistry, University at Buffalo, State University of New York, Buffalo, New York 14260, USA.lld:pubmed
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