Proline catalyzed direct diastereoselective 6-enolexo aldolization: toward the synthesis of the imino sugar DNJ

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DC Field	Value	Language
dc.contributor.author	Kumar, Indresh	-
dc.date.accessioned	2021-10-27T04:28:24Z	-
dc.date.available	2021-10-27T04:28:24Z	-
dc.date.issued	2010-11	-
dc.identifier.uri	https://www.sciencedirect.com/science/article/pii/S0957416610007366?via%3Dihub	-
dc.identifier.uri	http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3184	-
dc.description.abstract	A l-proline catalyzed direct diastereoselective 6-enolexo aldolization reaction of differentiating dialdehydes derived from tartaric acid is presented. This organocatalytic approach provides high levels of syn-selectivity (dr >10:1) with the stereocontrolled C–C bond formation between C4 and C5 intramolecularly, which can serve to synthesize imino-sugar skeleton quickly.	en_US
dc.language.iso	en	en_US
dc.publisher	Elsiever	en_US
dc.subject	Chemistry	en_US
dc.subject	Proline catalyzed	en_US
dc.subject	Diastereoselective	en_US
dc.subject	Synthesis	en_US
dc.title	Proline catalyzed direct diastereoselective 6-enolexo aldolization: toward the synthesis of the imino sugar DNJ	en_US
dc.type	Article	en_US
Appears in Collections:	Department of Chemistry

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