Advanced search

Synthetic entry to functionalised morpholines and [1,4]-oxazepanes via reductive amination reactions of carbohydrate derived dialdehydes

Download
Full text not archived in this repository.
Advice

Please see our End User Agreement.

It is advisable to refer to the publisher's version if you intend to cite from this work. See Guidance on citing.

Tools
Add to AnyAdd to TwitterAdd to FacebookAdd to LinkedinAdd to PinterestAdd to Email
Lists

Clark, S.M. and Osborn, H.M.I. orcid id iconORCID: https://orcid.org/0000-0002-0683-0457 (2004) Synthetic entry to functionalised morpholines and [1,4]-oxazepanes via reductive amination reactions of carbohydrate derived dialdehydes. Tetrahedron-Asymmetry, 15 (22). pp. 3643-3652. ISSN 0957-4166 doi: 10.1016/j.tetasy.2004.10.002

Abstract/Summary

The rapid synthesis of functionalised morpholines and [1,4]-oxazepanes displaying up to three stereocentres, by reductive amination reactions between carbohydrate derived dialdehydes and a range of amines, is described. (C) 2004 Elsevier Ltd. All rights reserved.

Altmetric Badge

Item Type Article
URI https://reading-clone.eprints-hosting.org/id/eprint/11142
Identification Number/DOI 10.1016/j.tetasy.2004.10.002
Refereed Yes
Divisions Life Sciences > School of Chemistry, Food and Pharmacy > Department of Chemistry
Uncontrolled Keywords POTENT GLYCOSIDASE INHIBITORS, SELECTIVE REDUCING AGENT, GLYCOL, FISSION, RIGID SYSTEMS, D-GLUCOSE, DERIVATIVES, RING, MONOSACCHARIDES, SYNTHONS, ANALOGS
Download/View statistics View download statistics for this item
Deposit Details

University Staff: Request a correction | Centaur Editors: Update this record

Search Google Scholar