Convenient methods to access chiral camphanyl amine derivatives by sodium borohydride reduction of d -(-)-camphorquinone imines

dc.contributor.author	Periasamy, Mariappan
dc.contributor.author	Sanjeevakumar, Nalluri
dc.contributor.author	Reddy, Polimera Obula
dc.date.accessioned	2022-03-27T09:07:12Z
dc.date.available	2022-03-27T09:07:12Z
dc.date.issued	2012-08-22
dc.description.abstract	d-(-)-Camphorquinone imines prepared using methanolic ammonia, ethanol amine, exo-(-)-bornylamine, ethylene diamine, propylene diamine, and trans-(R,R)-1,2-diaminocyclohexane, upon reduction using sodium borohydride in methanol, give the corresponding chiral exo amino alcohol and diamine derivatives in good yields (75-95%). © 2012 Georg Thieme Verlag Stuttgart New York.
dc.identifier.citation	Synthesis (Germany). v.44(20)
dc.identifier.issn	00397881
dc.identifier.uri	10.1055/s-0032-1317012
dc.identifier.uri	http://www.thieme-connect.de/DOI/DOI?10.1055/s-0032-1317012
dc.identifier.uri	https://dspace.uohyd.ac.in/handle/1/12446
dc.subject	chirality
dc.subject	diamines
dc.subject	diimines
dc.subject	reduction
dc.subject	sodium borohydride
dc.title	Convenient methods to access chiral camphanyl amine derivatives by sodium borohydride reduction of d -(-)-camphorquinone imines
dc.type	Journal. Article
dspace.entity.type

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