Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Jakob Blom"'
Autor:
Carlo Burkhardt, Francisco Ortiz, Kaies Daoud, Tomas Björnfot, Fredrik Ahrentorp, Jakob Blomgren, Allan Walton
Publikováno v:
Magnetism, Vol 4, Iss 3, Pp 295-304 (2024)
This work describes an automated pilot plant for the extraction of rare-earth (RE) permanent magnets from computer hard-disk drives (HDDs), demonstrating a commercially viable way to exploit these abundant sources of end-of-life (EOL) magnets. A mobi
Externí odkaz:
https://doaj.org/article/4744ead86c534a97a002fede1dfa4f11
Autor:
Jakob Blom, Lisa-Marie Mohr, Karl Anker Jørgensen, Johannes N. Lamhauge, Christina H. McCulley
Publikováno v:
Mohr, L M, McCulley, C H, Blom, J, Lamhauge, J N & Anker Jørgensen, K 2021, ' Investigation of the Organocatalytic Chlorination of 2-Phenylpropanal ', Chemistry-A European Journal, vol. 27, no. 69, pp. 17465-17475 . https://doi.org/10.1002/chem.202103376
Results of an examination of the organocatalytic enantioselective α-chlorination of 2-phenylpropanal are described. Synthetic investigation including the screening of primary and secondary aminocatalysts, many different reaction conditions, and othe
Autor:
Matilde Rusbjerg, Jakob Blom, Casper L. Barløse, Karl Anker Jørgensen, Henriette N. Tobiesen, Marc V. Iversen, Niels Hammer, Gabriel J. Reyes-Rodríguez, Johannes N. Lamhauge
Publikováno v:
Blom, J, Reyes Rodriguez, G J, Tobiesen, H N, Lamhauge, J N, Iversen, M V, Barløse, C L, Hammer, N, Rusbjerg, M & Jørgensen, K A 2019, ' Umpolung Strategy for α-Functionalization of Aldehydes for the Addition of Thiols and other Nucleophiles ', Angewandte Chemie-International Edition, vol. 58, no. 49, pp. 17856-17862 . https://doi.org/10.1002/anie.201911793
Nucleophile–nucleophile coupling is a challenging transformation in organic chemistry. Herein we present a novel umpolung strategy for α-functionalization of aldehydes with nucleophiles. The strategy uses organocatalytic enamine activation and qui
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6637934f6e9d01618a42daf47b29a1e2
https://pure.au.dk/portal/da/publications/umpolung-strategy-for-functionalization-of-aldehydes-for-the-addition-of-thiols-and-other-nucleophiles(392d5730-182a-4517-8029-cd1380085d7f).html
https://pure.au.dk/portal/da/publications/umpolung-strategy-for-functionalization-of-aldehydes-for-the-addition-of-thiols-and-other-nucleophiles(392d5730-182a-4517-8029-cd1380085d7f).html
Publikováno v:
Blom, J, Johansen, T K, Jensen, F & Jørgensen, K A 2016, ' Dynamic resolution of 2-cyclohexylidene acetaldehydes through organocatalytic dienamine [4+2] cycloaddition ', Chemical Communications, vol. 52, no. 44, pp. 7153-7156 . https://doi.org/10.1039/c6cc02019d
Organocatalytic formed dienamines are shown to be involved in dynamic resolution of 2-cyclohexylidene acetaldehydes. By reaction of racemic 2-cyclohexylidene acetaldehydes with benzoquinones in the presence of a diarylprolinol-silyl ether catalyst, t
Autor:
Karl Anker Jørgensen, Jakob Blom, Marc V. Iversen, Julie Jørgensen, Casper L. Barløse, Kamilla S. Jessen, Andreu Vidal-Albalat
Publikováno v:
Blom, J, Vidal-Albalat, A, Jørgensen, J, Barløse, C L, Jessen, K S, Iversen, M V & Jørgensen, K A 2017, ' Directing the Activation of Donor–Acceptor Cyclopropanes Towards Stereoselective 1,3-Dipolar Cycloaddition Reactions by Brønsted Base Catalysis ', Angewandte Chemie-International Edition, vol. 56, no. 39, pp. 11831-11835 . https://doi.org/10.1002/anie.201706150
The first stereoselective organocatalyzed [3+2] cycloaddition reaction of donor-acceptor cyclopropanes is presented. It is demonstrated that by applying an optically active bifunctional Brønsted base catalyst, racemic di-cyano cyclopropylketones can
Publikováno v:
Næsborg, L, Tur Espinosa, F, Meazza, M, Blom, J, Halskov, K S & Jørgensen, K A 2017, ' Synergistic Catalysis for the Asymmetric [3+2] Cycloaddition of Vinyl Aziridines with α,β-Unsaturated Aldehydes ', Chemistry: A European Journal, vol. 23, no. 2, pp. 268-272 . https://doi.org/10.1002/chem.201604995
The first asymmetric [3+2] cycloaddition of vinyl aziridines with alpha,beta-unsaturated aldehydes, based on synergistic catalysis, is disclosed. This methodology allows for the formation of attractive pyrrolidine structures in good yields (up to 84%
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78c697ba9d94d6bb35eb12658f80d2d3
https://pure.au.dk/portal/da/publications/synergistic-catalysis-for-the-asymmetric-32-cycloaddition-of-vinyl-aziridines-with-unsaturated-aldehydes(0455dea5-19c4-446d-b607-391a33844e53).html
https://pure.au.dk/portal/da/publications/synergistic-catalysis-for-the-asymmetric-32-cycloaddition-of-vinyl-aziridines-with-unsaturated-aldehydes(0455dea5-19c4-446d-b607-391a33844e53).html
Publikováno v:
ChemInform. 47
Publikováno v:
Lauridsen, V H, Ibsen, L, Blom, J & Jørgensen, K A 2016, ' Asymmetric Brønsted Base Catalyzed and Directed [3+2] Cycloaddition of 2-Acyl Cycloheptatrienes with Azomethine Ylides ', Chemistry: A European Journal, vol. 22, no. 10, pp. 3259-3263 . https://doi.org/10.1002/chem.201600255
Conjugated cyclic trienes have the potential for different types of cycloaddition reactions. In the present work, we will, in a novel asymmetric cycloaddition reaction, demonstrate that the organocatalytic reaction of 2-acyl cycloheptatrienes with az
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cea38aef77ce50092514e6c97896ef33
https://pure.au.dk/portal/da/publications/asymmetric-broensted-base-catalyzed-and-directed-32-cycloaddition-of-2acyl-cycloheptatrienes-with-azomethine-ylides(36385bbf-eb2c-49b9-b96a-26b64e46d79b).html
https://pure.au.dk/portal/da/publications/asymmetric-broensted-base-catalyzed-and-directed-32-cycloaddition-of-2acyl-cycloheptatrienes-with-azomethine-ylides(36385bbf-eb2c-49b9-b96a-26b64e46d79b).html
Autor:
Jakob Blom, Carl Olof Rosted
Publikováno v:
Acta chemica Scandinavica. 1(1)
Publikováno v:
Frontiers in Big Data, Vol 4 (2021)
The past years have shown a revolution in the way scientific workloads are being executed thanks to the wide adoption of software containers. These containers run largely isolated from the host system, ensuring that the development and execution envi
Externí odkaz:
https://doaj.org/article/cc8fed980b324342995cf10da025c49b