Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Eirik Johansson Solum"'
Autor:
Yasser Mohamed, Eirik Johansson Solum
Publikováno v:
ARKIVOC, Vol 2017, Iss 5, Pp 10-19 (2017)
Externí odkaz:
https://doaj.org/article/aa37a19cd02e4d019feaac066345371e
Autor:
Karoline Gangestad Primdahl, Frederik André Hansen, Eirik Johansson Solum, Jens Mortansson Jelstrup Nolsøe, Marius Aursnes
Publikováno v:
Journal of Chemical Education. 99:2372-2377
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27de0160ac28fd5ce4b7f9eab71a4502
https://doi.org/10.1021/acs.jchemed.1c00917
https://doi.org/10.1021/acs.jchemed.1c00917
Publikováno v:
SSRN Electronic Journal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99cbe60e2341f400ad56fca00a593c37
https://doi.org/10.2139/ssrn.4210991
https://doi.org/10.2139/ssrn.4210991
Publikováno v:
Steroids. 178
Five new compounds based on the structure of ergosterol have been prepared and tested for their ability to inhibit CDK8. The design of the compounds was inspired by the previous reported CDK8 inhibitors, cortistatin A, CCT251921 and Senexin A. The tw
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5fadffba87d5bad0685798539c4dfd1
https://pubmed.ncbi.nlm.nih.gov/35065996
https://pubmed.ncbi.nlm.nih.gov/35065996
Publikováno v:
Synthetic Communications. 49:1159-1164
An efficient stereoselective synthesis 3α- and 3β-aminoandrostan-17-one and 3α-amino dehydroepiandrosten-17-one based on a Mitsunobu reaction has been developed, using azide as the ammonia equivale...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b073b9d49e2c77b4ccd39e08a74e137d
https://doi.org/10.1080/00397911.2019.1590602
https://doi.org/10.1080/00397911.2019.1590602
Publikováno v:
Molecules
Volume 25
Issue 13
Molecules, Vol 25, Iss 3052, p 3052 (2020)
Volume 25
Issue 13
Molecules, Vol 25, Iss 3052, p 3052 (2020)
The synthesis, cytotoxicity and inhibition of CDK8 by thirteen analogs of cortistatin A are reported. These efforts revealed that the analogs with either a 6- or 7-isoquinoline or 5-indole side chain in the 17-position are the most promising anti-pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3cc506094bf6e2b0e7726666d474e359
http://europepmc.org/articles/PMC7412091
http://europepmc.org/articles/PMC7412091
Publikováno v:
Current organic synthesis. 18(1)
The implementation of heterogeneous photo-nanocatalysts in organic syntheses has been investigated greatly in the last decade as a result of the increasing demand to achieve the organic reactions via the use of green approaches and through the availa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4dcf36ff24ac8028d5049cfa829e8f4
https://pubmed.ncbi.nlm.nih.gov/33019933
https://pubmed.ncbi.nlm.nih.gov/33019933
Publikováno v:
Bioorganic & Medicinal Chemistry
28:115461
28:115461
Cyclin-dependent kinase 8 (CDK8) plays a vital role in regulating cell transcription either through its association with the mediator complex or by the phosphorylation of transcription factors. CDK8-mediated activation of oncogenes has proved to be i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebbbb14f67ce1697de80895df3b62697
https://hdl.handle.net/11250/2661805
https://hdl.handle.net/11250/2661805
Publikováno v:
Chemical Papers. 73:435-445
Herein we report the use of Ag/TiO2 and Pt/TiO2 nanocatalysts to promote the synthesis of a series of silyl-protected and functionalized propargylamine derivatives through alkyne–amine–aldehyde (A3) coupling under microwave condition using water
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d0ae25d07aca1e2a4c9815b2bed7c24
https://doi.org/10.1007/s11696-018-0604-6
https://doi.org/10.1007/s11696-018-0604-6
Publikováno v:
Monatshefte für Chemie - Chemical Monthly. 149:1857-1864
Palladium-catalyzed, cross-coupling reaction of N-methyl-3-iodo-4-quinolone with boronic acids or N-methyliminodiacetic acid boronates to obtain azaisoflavone derivatives was investigated through conventional Suzuki–Miyuara coupling or by slow rele
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::195bb8a8bddc76cad5e374efc2fff717
https://doi.org/10.1007/s00706-018-2252-5
https://doi.org/10.1007/s00706-018-2252-5