Bhaumik, Atanu ; Pal, Tarun Kumar ; Pathak, Tanmaya (2015) 1,1-Dioxothiomorpholines with asymmetric environments: protecting group directed diastereoselectivity of glyco divinyl sulfone cyclization RSC Advances, 5 (35). pp. 27706-27710. ISSN 2046-2069
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Official URL: http://pubs.rsc.org/en/Content/ArticleLanding/2015...
Related URL: http://dx.doi.org/10.1039/C5RA03276H
Abstract
Divinyl sulfones derived from pyranoside skeletons afforded 1,1-dioxothiomorpholine with predefined asymmetric environments. Although the exocyclic vinyl sulfone group easily reacts with primary amines, the intramolecular addition pattern of the secondary amine leading to the formation of the 1,1-dioxothiomorpholine derivative dramatically varied when benzylidene protection was replaced by benzyl protecting groups.
Item Type: | Article |
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Source: | Copyright of this article belongs to Royal Society of Chemistry. |
ID Code: | 103743 |
Deposited On: | 22 Mar 2017 05:12 |
Last Modified: | 22 Mar 2017 05:12 |
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