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Data · dataset · 2015

The first general protocol for N -monoalkylation of sulfamate esters: benign synthesis of N -alkyl Topiramate (anticonvulsant drug) derivatives

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A novel protocol for the highly selective N -monoalkylation of the sulfamate ester moiety has been developed.

Description

This reaction proceeded efficiently using alkyl halides, benzyl halides and α-halo ketones as the electrophile in the presence of KF-Al 2 O 3 as a cost-effective and robust catalyst. This approach provides new access to N -monoalkylated Topiramate (anticonvulsant drug) derivatives which are potentially of great importance in medicinal chemistry.

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Provenance · 1 source records, 12 field assertions
SourceKeyLast seenRaw
DataCite10.6084/m9.figshare.149659114 d agoJSON v1
FieldAssertionExtractorEvidence
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concepts[field].local:field:chemistrymapping · DataCitevocabulary-mapper@1.0.0keywords['Chemistry']
concepts[field].local:field:life-sciencesmapping · DataCitevocabulary-mapper@1.0.0keywords['Biological Sciences']
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