alexa Synthesis Of Aminocyclopetitol Analogues Via CSI-mediated Stereoselective Amination
ISSN: 2161-0401

Organic Chemistry: Current Research
Open Access

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2nd European Organic Chemistry Congress
March 02-03, 2017 Amsterdam, Netherlands

Han Pyo Son, Yeon Su Kim, Sook Jin Park, Jun Min Jung and Young Hoon Jung
Sungkyunkwan University, South Korea
Posters & Accepted Abstracts: Organic Chem Curr Res
DOI: 10.4172/2161-0401.C1.017
Recent years have witnessed a great deal of attention in the preparation and biological evaluation of carbocyclic amino alcohols, which either exist in nature or constitute crucial core structures of several natural products. This class of molecules involves two typical substructures such as aminocyclopentitol and aminocyclohexitol. Among the well-known examples of aminocyclopentitol are mannostatin A and trehazolin. Aminocyclopentitol scaffold has been also found in a range of carbocyclic nucleosides such as neplanocin A and its unsaturated analogue (–)-aristeromycin. Due to the absence of a true glycosidic bond, carbocyclic nucleosides are more chemically stable and not involved in the action of the enzymes that cleave the N-glycosidic linkage in conventional nucleosides. Thus carbocyclic amino alcohol moiety has been the focus of much attention in the development of new therapeutic agents. In this presentation, we describe a divergent synthesis of some novel aminocyclopentitol analogues was concisely achieved from readily available sugar via the highly diastereoselective amination of carbocyclic polybenzyl ether using chlorosulfonyl isocyanate, diastereoselective dihydroxylation, and epoxidation as the key steps.

Han Pyo Son is currently affiliated to the Sungkyunkwan University, South Korea.

Email: [email protected]

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