Direct catalytic synthesis of densely substituted 3-formylpyrroles from imines and 1,4-ketoaldehydes

dc.contributor.authorKumar, Indresh
dc.date.accessioned2021-10-27T04:27:54Z
dc.date.available2021-10-27T04:27:54Z
dc.date.issued2014
dc.description.abstractA sustainable method for the direct access to highly substituted 3-formylpyrroles from 1,4-ketoaldehydes and imine via formal [3 + 2] cycloaddition is reported. This reaction involves a one-pot amine catalyzed chemoselective Mannich-cyclization-aerobic oxidation sequence with good to high yields. Further application of the gram scale reaction as well as synthesis of fully substituted 3-formylpyrrole is also shown.en_US
dc.identifier.urihttps://pubs.rsc.org/en/content/articlelanding/2014/ra/c4ra06581f
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3173
dc.language.isoenen_US
dc.publisherRSCen_US
dc.subjectChemistryen_US
dc.subjectSynthesisen_US
dc.subject3-formylpyrrolesen_US
dc.subjectKetoaldehydesen_US
dc.titleDirect catalytic synthesis of densely substituted 3-formylpyrroles from imines and 1,4-ketoaldehydesen_US
dc.typeArticleen_US

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