Mimicking dihydroxy acetone phosphate-utilizing aldolases through organocatalysis: A facile route to carbohydrates and aminosugars

dc.contributor.author	Suri, Jeff T.
dc.contributor.author	Ramachary, Dhevalapally B.
dc.contributor.author	Barbas, Carlos F.
dc.date.accessioned	2022-03-27T09:42:37Z
dc.date.available	2022-03-27T09:42:37Z
dc.date.issued	2005-03-31
dc.description.abstract	(Chemical Equation Presented) A practical and environmentally friendly organocatalytic strategy designed to mimic the DHAP aldolases has been developed and shown to be effective in the preparation of carbohydrates and aminosugars. (S)-Proline and (S)-2-pyrrolidine-tetrazole catalyzed the aldol reaction between dihydroxy acetone variants such as 1,3-dioxan-5-one and 2,2-dimethyl-1,3- dioxan-5-one with aldehydes to give the corresponding polyols in good yields with very high ees. © 2005 American Chemical Society.
dc.identifier.citation	Organic Letters. v.7(7)
dc.identifier.issn	15237060
dc.identifier.uri	10.1021/ol0502533
dc.identifier.uri	https://pubs.acs.org/doi/10.1021/ol0502533
dc.identifier.uri	https://dspace.uohyd.ac.in/handle/1/13222
dc.title	Mimicking dihydroxy acetone phosphate-utilizing aldolases through organocatalysis: A facile route to carbohydrates and aminosugars
dc.type	Journal. Article
dspace.entity.type

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