Zobrazeno 1 - 10
of 288
pro vyhledávání: '"Mikael Bols"'
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:
Mikael Bols, Christian Marcus Pedersen
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 13, Iss 1, Pp 93-105 (2017)
Silyl groups such as TBDPS, TBDMS, TIPS or TMS are well-known and widely used alcohol protective groups in organic chemistry. Cyclic silylene protective groups are also becoming increasingly popular. In carbohydrate chemistry silyl protective groups
Externí odkaz:
https://doaj.org/article/3d96db2bbeb94359854545ac1060cf97
Autor:
Marité Cárdenas, Christian M. Pedersen, Vivien Jagalski, Mikael Bols, Thomas G. Pomorski, Wouter F. J. Hogendorf
Publikováno v:
Molecules, Vol 18, Iss 11, Pp 13546-13573 (2013)
Four glycoglycerolipids with different head groups have been synthesized and their physicochemical properties studied. The lengths of the head groups from a mono-saccharide to a trisaccharide, in addition to the anomeric stereochemistry for the small
Externí odkaz:
https://doaj.org/article/a6653681256442aeb543259fd2f5e8e6
Publikováno v:
ARKIVOC, Vol 2013, Iss 2, Pp 249-275 (2012)
Externí odkaz:
https://doaj.org/article/96e032a990034c7ea40c9fdfea477cb0
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:
Yousefi, N-A, Zimmermann, M L & Bols, M 2022, ' A study of the DIBAL-promoted selective debenzylation of alpha-cyclodextrin protected with two different benzyl groups ', Beilstein Journal of Organic Chemistry, vol. 18, pp. 1553-1559 . https://doi.org/10.3762/bjoc.18.165
An α-cyclodextrin protected with 2,4-dichlorobenzyl groups on the primary alcohols and ordinary benzyl groups on the secondary alcohols was prepared and subjected to DIBAL (diisobutylaluminum hydride)-promoted selective debenzylation. Debenzylation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13d9adad42a2a7cbf668a1b122a1ddd3
https://curis.ku.dk/portal/da/publications/a-study-of-the-dibalpromoted-selective-debenzylation-of-alphacyclodextrin-protected-with-two-different-benzyl-groups(045a22ad-e58f-4583-bbe0-1eaad4e14401).html
https://curis.ku.dk/portal/da/publications/a-study-of-the-dibalpromoted-selective-debenzylation-of-alphacyclodextrin-protected-with-two-different-benzyl-groups(045a22ad-e58f-4583-bbe0-1eaad4e14401).html
Publikováno v:
European Journal of Organic Chemistry. 2020:3989-3996
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2aed0dac463249c3dd4d4b5e59d7e57d
https://doi.org/10.1002/ejoc.202000522
https://doi.org/10.1002/ejoc.202000522
Autor:
Francesca Cardona, Mikael Bols, Bo Wang, Andrea Goti, Camilla Matassini, Amelia Morrone, Julia Warren
Publikováno v:
Angewandte Chemie. 132:10552-10555
Gaucher disease is caused by mutations in human acid β-glucosidase or glucocerebrosidase (GCase), the enzyme responsible for hydrolysis of glucosyl ceramide in the lysosomes. Imino- and azasugars such as 1-deoxynojirimycin and isofagomine are strong
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25e1c48a558bc048453bce1c0d6a23ab
https://doi.org/10.1002/ange.202002850
https://doi.org/10.1002/ange.202002850
Autor:
Mikael Bols, Victor Friis
Publikováno v:
Bols, M & Friis, V 2022, ' Taming of the DIBAL Promoted Debenzylation of α-Cyclodextrin. Kinetics, Substituent Effects and Efficient Synthesis of Lings Tetrol** ', Chemistry-A European Journal, vol. 28, no. 29, e202200564 . https://doi.org/10.1002/chem.202200564
The kinetics of the reaction of perbenzyl α-cyclodextrin was studied varying the concentration of DIBAL and substrate, and the temperature. The initial debenzylation was found to be 1st order in substrate and follow the relationship 0.0675+0.179[DIB
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a681986de1321b7fbdb922854d2654d
https://curis.ku.dk/portal/da/publications/taming-of-the-dibal-promoted-debenzylation-of-cyclodextrin-kinetics-substituent-effects-and-efficient-synthesis-of-lings-tetrol(24f95e2e-b421-479d-9d15-69fda67e8ef3).html
https://curis.ku.dk/portal/da/publications/taming-of-the-dibal-promoted-debenzylation-of-cyclodextrin-kinetics-substituent-effects-and-efficient-synthesis-of-lings-tetrol(24f95e2e-b421-479d-9d15-69fda67e8ef3).html
Autor:
Jacob Valdbjørn Olsen, Morten Meldal, Morten Petersen, Frederik Præstholm Jørgensen, Daniel H. Madsen, Mikael Bols, Jeppe Granhøj
Publikováno v:
Journal of Medicinal Chemistry. 62:5191-5216
A series of 35 analogues of Shld with modifications in the A-residue and the C-residues were prepared and investigated for binding to FKBP and GFP accumulation in transgenic plants. The modifications investigated explored variations that were suppose
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95317feca6c76645dbea037e1e98d4df
https://doi.org/10.1021/acs.jmedchem.9b00497
https://doi.org/10.1021/acs.jmedchem.9b00497