Aza variant of intramolecular nucleophile-catalyzed aldol lactonization (NCAL): formal synthesis of (3S, 4R) and (3R, 4S) 4-(hydroxymethyl) pyrrolidin-3-ol

Dikshit, D K; Sikriwal, Dimpy

dc.contributor.author	Dikshit, D K
dc.contributor.author	Sikriwal, Dimpy
dc.date.accessioned	2011-06-24T09:19:00Z
dc.date.available	2011-06-24T09:19:00Z
dc.date.issued	2011
dc.identifier.citation	Tetrahedron (2011), 67(17), 210-15	en
dc.identifier.uri	http://hdl.handle.net/123456789/691
dc.description.abstract	Aza variant of intramolecular catalytic, asymmetric nucleophile-catalyzed, aldol lactonization (NCAL) reaction has been explored to synthesize β-lactone fused nitrogen heterocyclics as aza-sugars precursors by employing achiral amino acids. The utility of these bicyclic β-lactones is presented by the formal synthesis of aza-sugars, (3S, 4R) and (3R, 4S) 4-(hydroxymethyl) pyrrolidin-3-ol	en
dc.format.extent	372833 bytes
dc.format.mimetype	application/pdf
dc.language.iso	en	en
dc.relation.ispartofseries	cdricommunication no.7983	en
dc.subject	Aza sugars	en
dc.subject	Aza NCAL reaction	en
dc.subject	Acetyl quinidine	en
dc.subject	β-lactone	en
dc.subject	O-Acetyl quinine	en
dc.title	Aza variant of intramolecular nucleophile-catalyzed aldol lactonization (NCAL): formal synthesis of (3S, 4R) and (3R, 4S) 4-(hydroxymethyl) pyrrolidin-3-ol	en
dc.type	Article	en