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The synthesis of chiral 5-methylene pyrrol-2(5H)-ones via photooxygenation of homochiral 2-methylpyrrole derivatives

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dc.contributor.authorDemir, AS
dc.contributor.authorAydogan, F
dc.contributor.authorAkhmedov, IM
dc.date.accessioned2026-06-27T12:59:17Z
dc.date.issued2002
dc.description.abstractHomochiral 2-methylpyrrole derivatives are synthesized in high yields starting from chiral amines, amino alcohols and amino acid esters. The photooxygenation of these pyrrole derivatives in the presence of a photosensitiser furnishes the corresponding alpha,beta,gamma,delta-unsaturated gamma-lactams as the major products in good yields. (C) 2002 Elsevier Science Ltd. All rights reserved.en
dc.description.urihttps://doi.org/10.1016/s0957-4166(02)00140-4
dc.identifier.doi10.1016/s0957-4166(02)00140-4
dc.identifier.endpage605
dc.identifier.issn0957-4166
dc.identifier.issue6
dc.identifier.startpage601
dc.identifier.urihttps://hdl.handle.net/20.500.14981/48611
dc.identifier.volume13
dc.identifier.wos000175678200007
dc.language.isoeng
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD
dc.relation.ispartofTETRAHEDRON-ASYMMETRY
dc.subjectSINGLET OXYGEN OXIDATION
dc.subjectPYRROLE
dc.subjectTRANSFORMATIONS
dc.subjectChemistry
dc.titleThe synthesis of chiral 5-methylene pyrrol-2(5H)-ones via photooxygenation of homochiral 2-methylpyrrole derivatives
dc.typeArticle
dspace.entity.typePublication
local.import.sourceWOS

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