Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Anna V. Gudmundsdottir"'
Publikováno v:
Marine Drugs, Vol 13, Iss 1, Pp 173-201 (2015)
This report describes the synthesis of reversed structured 1-O-alkyl-2,3-diacyl-sn-glycerols (DAGEs) possessing a pure saturated even number fatty acid (C6:0–C16:0) at the sn-2 position along with a pure EPA or DHA located at the terminal sn-3 posi
Externí odkaz:
https://doaj.org/article/68a7015f1b574d0ab0ce29b85537b485
Synthesis of reversed structured triacylglycerols possessing EPA and DHA at their terminal positions
Publikováno v:
Tetrahedron. 71:8544-8550
This report describes synthesis of reversed structured triacylglycerols (TAGs) of the LML type, possessing pure EPA or DHA located at the terminal 1,3-positions of the glycerol backbone along with pure even number saturated fatty acids (C6:0–C16:0)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f89d57c3f4490496ca83d1ef3e63c32
https://doi.org/10.1016/j.tet.2015.09.034
https://doi.org/10.1016/j.tet.2015.09.034
Publikováno v:
Marine Drugs, Vol 13, Iss 1, Pp 173-201 (2015)
Marine Drugs
Volume 13
Issue 1
Pages 173-201
Marine Drugs
Volume 13
Issue 1
Pages 173-201
This report describes the synthesis of reversed structured 1-O-alkyl-2,3-diacyl-sn-glycerols (DAGEs) possessing a pure saturated even number fatty acid (C6:0-C16:0) at the sn-2 position along with a pure EPA or DHA located at the terminal sn-3 positi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62da500f3e542a80258c7f17a85683a8
http://www.mdpi.com/1660-3397/13/1/173
http://www.mdpi.com/1660-3397/13/1/173
Publikováno v:
Carbohydrate Research. 344:278-284
Glycoconjugates can be readily formed by the condensation of a free-reducing terminus and a strong alpha-effect nucleophile, such as a hydrazide or a hydroxylamine. Further characterization of a series of glycoconjugates formed from xylose, glucose a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::464d04937fd788a39735529f63055fe3
https://doi.org/10.1016/j.carres.2008.11.007
https://doi.org/10.1016/j.carres.2008.11.007
Autor:
Anna V. Gudmundsdottir, Mark Nitz
Publikováno v:
Carbohydrate Research. 342:749-752
A series of substituted 1-glucosyl-2-benzoylhydrazines were synthesized and their pseudo-first-order rate constants for hydrolysis were determined at pH 4, 5, 6 at 50 degrees C. All the compounds hydrolyzed quickly (t(1/2)3h) at pH 4.0, but were incr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b51d099f74e6f03b3190437d372e6f7
https://doi.org/10.1016/j.carres.2006.12.015
https://doi.org/10.1016/j.carres.2006.12.015
Autor:
Anna V. Gudmundsdottir, Mark Nitz
Publikováno v:
Organic letters. 10(16)
N'-Glycopyranosylsulfonohydrazides are introduced as glycosyl donors for protecting group free synthesis of O-glycosides, glycosyl azides, and oxazolines. Mono- and disaccharides containing a reducing terminal N-acetylglucosamine residue were condens
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8719c367b7f8545423c8378f3f3dd3a
https://pubmed.ncbi.nlm.nih.gov/18616337
https://pubmed.ncbi.nlm.nih.gov/18616337
Publikováno v:
Tetrahedron. 71:9177
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4272e83ec1cb5cd232dfad2b49d9d79d
https://doi.org/10.1016/j.tet.2015.10.026
https://doi.org/10.1016/j.tet.2015.10.026