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Please use this identifier to cite or link to this item: http://10.10.120.238:8080/xmlui/handle/123456789/1018
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dc.contributor.authorTamannaen_US
dc.contributor.authorKumar M.en_US
dc.contributor.authorJoshi K.en_US
dc.contributor.authorChauhan P.en_US
dc.date.accessioned2023-11-30T09:01:28Z-
dc.date.available2023-11-30T09:01:28Z-
dc.date.issued2020-
dc.identifier.issn1615-4150-
dc.identifier.otherEID(2-s2.0-85083851391)-
dc.identifier.urihttps://dx.doi.org/10.1002/adsc.202000243-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/1018-
dc.description.abstractThe isochroman scaffold constitutes an important structural unit, which is present in various bioactive natural products and synthetic pharmaceutical compounds exhibiting wide arrays of biological properties. Hence the synthesis of this class of heterocyclic compounds in a stereoselective fashion is highly significant and desirable. In the last decade, a substantial advancement has been witnessed ln the catalytic asymmetric synthesis of isochroman derivatives by employing metal catalysts bearing chiral ligands or by chiral metal-free organocatalysts. This review aims to provide an overview of the transition metal-catalyzed and organocatalyzed asymmetric syntheses of isochroman derivatives including isochromenes and isochromanones. (Figure presented.). © 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheimen_US
dc.language.isoenen_US
dc.publisherWiley-VCH Verlagen_US
dc.sourceAdvanced Synthesis and Catalysisen_US
dc.subjectasymmetric catalysisen_US
dc.subjectisochromanonesen_US
dc.subjectisochromansen_US
dc.subjectisochromenesen_US
dc.subjectorganic catalysisen_US
dc.titleCatalytic Asymmetric Synthesis of Isochroman Derivativesen_US
dc.typeReviewen_US
Appears in Collections:Review

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