Synthesis of 5-(sulfamoylmethyl)indoles

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dc.contributor.authorJoan Bosch
dc.contributor.authorTomaÁs Roca
dc.contributor.authorMontserrat Armengol
dc.contributor.authorDolors FernaÂndez-Forner
dc.date.accessioned2012-11-09T10:08:50Z
dc.date.accessioned2025-02-17T13:59:37Z
dc.date.available2012-11-09T10:08:50Z
dc.date.issued2012-11-09
dc.descriptionThe synthesis of 5-(sulfamoylmethyl)indoles bearing a two-carbon chain at C-3 (aminoethyl, acetate, hydroxyethyl, ethyl) either by the Grandberg modi®cation of the Fischer indolization or by intramolecular Heck reaction of suitable o-halotri¯uoroacetanilides is reported. q 2001 Elsevier Science Ltd. All rights reserved.en_US
dc.description.abstractThe synthesis of 5-(sulfamoylmethyl)indoles bearing a two-carbon chain at C-3 (aminoethyl, acetate, hydroxyethyl, ethyl) either by the Grandberg modi®cation of the Fischer indolization or by intramolecular Heck reaction of suitable o-halotri¯uoroacetanilides is reported. q 2001 Elsevier Science Ltd. All rights reserveden_US
dc.identifier.urihttps://dl.ftveti.edu.et/handle/123456789/3986
dc.language.isoenen_US
dc.subjectThe synthesis of 5-(sulfamoylmethyl)indoles bearing a two-carbon chain at C-3 (aminoethyl, acetate, hydroxyethyl, ethyl) either by the Grandberg modi®cation of the Fischer indolization or by intramolecular Heck reaction of suitable o-halotri¯uoroacetanilides is reported. q 2001 Elsevier Science Ltd. All rights reserveden_US
dc.titleSynthesis of 5-(sulfamoylmethyl)indolesen_US
dc.typeArticleen_US

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