Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Martin Jaeger Pedersen"'
Autor:
Cecilie Høgfeldt Jessen, Jesper Bendix, Theis Brock Nannestad, Heloisa Bordallo, Martin Jæger Pedersen, Christian Marcus Pedersen, Mikael Bols
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 19, Iss 1, Pp 1021-1027 (2023)
Carbon dioxide (CO2) emissions from industrial processes, power generation, and transportation contribute significantly to global warming and climate change. Carbon capture and storage (CCS) technologies are essential to reduce these emissions and mi
Externí odkaz:
https://doaj.org/article/6313e4cae85a47bcabe40c61bc59e5e5
Autor:
Francisco J. Medrano, Mare Cudic, Hans-Joachim Gabius, Mark Reihill, Antonio A. Romero, Forrest G FitzGerald, Tammo Diercks, Donella Beckwith, Stefan Oscarson, Martin Jaeger Pedersen, Anna-Kristin Ludwig
Publikováno v:
Chemistry (Weinheim an Der Bergstrasse, Germany)
Digital.CSIC. Repositorio Institucional del CSIC
instname
Digital.CSIC. Repositorio Institucional del CSIC
instname
10 p.-6 fig.-3 tb.
Functional pairing between cellular glyco-con-ju-gates and tissue lectins like galectins has wide (patho)physio-logical significance. Their study is facilitated by non-hydrolyzable deri-va-tives of the natural O-glycans, such
Functional pairing between cellular glyco-con-ju-gates and tissue lectins like galectins has wide (patho)physio-logical significance. Their study is facilitated by non-hydrolyzable deri-va-tives of the natural O-glycans, such
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c376d7f6b08ab469bba1303caa4750ac
https://doi.org/10.1002/chem.202003143
https://doi.org/10.1002/chem.202003143
Publikováno v:
Synlett. 33:415-428
Silicon has been used in carbohydrate chemistry for half a century, but mostly as a protective group for sugar alcohols. Recently, the use of silicon has expanded to functionalization via C–H activation, conformational arming of glycosyl donors, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::db7554d67846ea161d51e51fed4e7ed1
https://doi.org/10.1055/s-0040-1719854
https://doi.org/10.1055/s-0040-1719854
Publikováno v:
Angewandte Chemie International Edition. 60:2689-2693
A method for introducing dimethylphenylsilyl at the 4-position in carbohydrates has been developed. Two C-silylated glycosyl donors were prepared via levoglucosenone, starting from cellulose. The glycosylation properties were studied using three gluc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8bd4d198d09050e14dc473aae22f85c
https://doi.org/10.1002/anie.202009209
https://doi.org/10.1002/anie.202009209
Publikováno v:
Angewandte Chemie. 133:2721-2725
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6fe9f677423862fdd29fa766d4ef0e4d
https://doi.org/10.1002/ange.202009209
https://doi.org/10.1002/ange.202009209
Publikováno v:
Green Chemistry. 22:2399-2402
Hydroxymethyl furanoic acid and its derivatives have been synthesized in high yields and purity from gluconolactone. The reaction sequence allows the recovery of reagents and the use of bio-friendly chemicals and solvents, and can easily be scaled up
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::52ebe1fb704d2649f1ae8dcd69a4209e
https://doi.org/10.1039/d0gc00770f
https://doi.org/10.1039/d0gc00770f
Publikováno v:
Pedersen, M J, Madsen, R & Clausen, M H 2018, ' Iridium Catalysis: Reductive Conversion of Glucan to Xylan ', Chemical Communications, vol. 54, no. 8, pp. 952-955 . https://doi.org/10.1039/C7CC09260A
By using iridium catalysed dehydrogenative decarbonylation, we converted a partly protected cellobioside into a fully protected xylobioside. We demonstrate good yields with two different aromatic ester protecting groups. The resulting xylobioside was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c492f636e1ea24b25903e590f3809e5
https://doi.org/10.1039/c7cc09260a
https://doi.org/10.1039/c7cc09260a