Pal, Rita and Das, Anupama and Jayaraman, Narayanaswamy (2018) Radical halogenation-mediated latent-active glycosylations of allyl glycosides. In: CHEMICAL COMMUNICATIONS, 54 (6). pp. 588-590.
Full text not available from this repository. (Request a copy)
Official URL: http://dx.doi.org/10.1039/c7cc07332a
Abstract
Radical halogenation-mediated glycosylation using allyl glycosides as donors and as acceptors emerges to be an efficient and hither-to unknown glycosylation method, adhering to the concept of the latent-active methodology. Several di- and trisaccharides that possess the allyl moiety at their reducing end are prepared through this new glycosylation methodology.
Item Type: | Journal Article |
---|---|
Publication: | CHEMICAL COMMUNICATIONS |
Additional Information: | Copy right for this article belong to the ROYAL SOC CHEMISTRY, THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND |
Department/Centre: | Division of Chemical Sciences > Organic Chemistry |
Date Deposited: | 02 Mar 2018 15:06 |
Last Modified: | 02 Mar 2018 15:06 |
URI: | http://eprints.iisc.ac.in/id/eprint/58911 |
Actions (login required)
View Item |