Stereoselective synthesis of 2-amino-1,3,5-hexane triols using l-proline catalyzed aldol reaction

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dc.contributor.authorKumar, Indresh
dc.date.accessioned2021-10-27T04:14:07Z
dc.date.available2021-10-27T04:14:07Z
dc.date.issued2006-03
dc.description.abstractAn efficient synthesis of the 2-amino-1,3,5-hexane triol pattern has been achieved by a diastereoselective aldol reaction of an amino aldehyde with acetone catalyzed by l-proline.en_US
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0957416606001194
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2999
dc.language.isoenen_US
dc.publisherElsieveren_US
dc.subjectChemistryen_US
dc.subjectStereoselectiveen_US
dc.subjectSynthesisen_US
dc.subjectl-proline catalyzeden_US
dc.titleStereoselective synthesis of 2-amino-1,3,5-hexane triols using l-proline catalyzed aldol reactionen_US
dc.typeArticleen_US

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