| dc.contributor.author | Vlahov, Iontcho R. | |
| dc.contributor.author | Linhardt, Robert J. | |
| dc.date | 1995 | |
| dc.date.accessioned | 2022-06-27T17:13:46Z | |
| dc.date.available | 2022-06-27T17:13:46Z | |
| dc.date.issued | 1995-11-13 | |
| dc.identifier.citation | Regioselective Synthesis of Derivatives of L-Idopyranuronic Acid: A Key Constituent of Glycosaminoglycans, I. R. Vlahov, R. J. Linhardt, Tetrahedron Letters, 36, 8379-8382, 1995. | |
| dc.identifier.issn | 404039 | |
| dc.identifier.uri | https://doi.org/10.1016/0040-4039(95)01810-5 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.13015/5942 | |
| dc.description | Tetrahedron Letters, 36, 8379-8382 | |
| dc.description | Note : if this item contains full text it may be a preprint, author manuscript, or a Gold OA copy that permits redistribution with a license such as CC BY. The final version is available through the publisher’s platform. | |
| dc.description.abstract | Synthesis of new and potentially universal l-idopyranuronic glycosyl-donor and/or -acceptor 13 was performed starting from d-glucofuranurono-6,3-lactone 1. After simple C-5-epimerization, C-1thioacetalization and regioselective p-methoxybenzylidenation to the hydroxylactone 6, the lactone ring was opened. The resulting diolamide stereoselectively protected, providing compound 7. Regioselective reductive cleavage of the 1,3-dioxane ring and subsequent deprotection afforded the target molecule 13. | |
| dc.description.uri | https://login.libproxy.rpi.edu/login?url=https://doi.org/10.1016/0040-4039(95)01810-5 | |
| dc.language | en_US | |
| dc.language.iso | ENG | |
| dc.relation.ispartof | The Linhardt Research Labs Online Collection | |
| dc.relation.ispartof | Rensselaer Polytechnic Institute, Troy, NY | |
| dc.relation.ispartof | Tetrahedron Letters | |
| dc.relation.uri | https://harc.rpi.edu/ | |
| dc.subject | Biology | |
| dc.subject | Chemistry and chemical biology | |
| dc.subject | Chemical and biological engineering | |
| dc.subject | Biomedical engineering | |
| dc.title | Regioselective Synthesis of Derivatives of L-Idopyranuronic Acid: A Key Constituent of Glycosaminoglycans | |
| dc.type | Article | |
| dcterms.accessRights | https://login.libproxy.rpi.edu/login?url=https://doi.org/10.1016/0040-4039(95)01810-5 | |
| dcterms.isPartOf | Journal | |
| dcterms.isVersionOf | https://doi.org/10.1016/0040-4039(95)01810-5 | |
| dc.rights.holder | In Copyright : this Item is protected by copyright and/or related rights. You are free to use this Item in any way that is permitted by the copyright and related rights legislation that applies to your use. For other uses you need to obtain permission from the rights-holder(s). https://rightsstatements.org/page/InC/1.0/ | |
| dc.creator.identifier | https://orcid.org/0000-0003-2219-5833 | |
| dc.relation.department | The Linhardt Research Labs. | |
| dc.relation.department | The Shirley Ann Jackson, Ph.D. Center for Biotechnology and Interdisciplinary Studies (CBIS) | |
| rpi.description.pages | 8379-8382 | |
| rpi.description.volume | 36 | |
