Construction of Isoxazolidines through Formal [3+2] Cycloaddition Reactions of in situ Generated Nitrosocarbonyls with Donor–Acceptor Cyclopropanes: Synthesis of α-Amino γ-Butyrolactones

Please use this identifier to cite or link to this item: http://dspace.iitrpr.ac.in:8080/xmlui/handle/123456789/363

Full metadata record

DC Field	Value	Language
dc.contributor.author	Varshnaya, R.K.	-
dc.contributor.author	Baneerji, P.	-
dc.date.accessioned	2016-11-16T11:23:21Z	-
dc.date.available	2016-11-16T11:23:21Z	-
dc.date.issued	2016-11-16	-
dc.identifier.uri	http://localhost:8080/xmlui/handle/123456789/363	-
dc.description.abstract	A straightforward approach for the synthesis of isoxazolidines through MgI2-catalyzed [3+2] cycloaddition reactions of donor–acceptor cyclopropanes with in situ generated nitrosocarbonyls from hydroxycarbamates is described. This method facilitates one-pot synthesis of α-amino-γ-butyrolactone by deprotection, reductive cleavage of N–O bond, and successive lactonization.	en_US
dc.language.iso	en_US	en_US
dc.title	Construction of Isoxazolidines through Formal [3+2] Cycloaddition Reactions of in situ Generated Nitrosocarbonyls with Donor–Acceptor Cyclopropanes: Synthesis of α-Amino γ-Butyrolactones	en_US
dc.type	Article	en_US
Appears in Collections:	Year-2016

Files in This Item:

File	Description	Size	Format
Full Text.pdf		1.16 MB	Adobe PDF	View/Open Request a copy

DSpace JSPUI