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pro vyhledávání: '"Huck, K."'
Akademický článek
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Autor:
Abu Hejleh, AP1,2 (AUTHOR), Huck, K1,2 (AUTHOR), Jähne, K1,2 (AUTHOR), Tan, CL2 (AUTHOR), Lanz, TV1,3 (AUTHOR), Epping, L4 (AUTHOR), Sonner, JK5 (AUTHOR), Meuth, SG4,6 (AUTHOR), Henneberg, A7,8 (AUTHOR), Opitz, CA7 (AUTHOR), Herold-Mende, C9 (AUTHOR), Sahm, F10,11 (AUTHOR), Platten, M1,2 (AUTHOR), Sahm, K1,2 (AUTHOR) Katharina.Sahm@umm.de
Publikováno v:
International Journal of Tryptophan Research. 2/9/2023, p1-11. 11p.
Autor:
Abu Hejleh, AP, Huck, K, Jähne, K, Tan, CL, Lanz, TV, Epping, L, Sonner, JK, Meuth, SG, Henneberg, A, Opitz, CA, Herold-Mende, C, Sahm, F, Platten, M, Sahm, K
Supplemental material, sj-docx-1-try-10.1177_11786469231153111 for Endothelial Indoleamine-2,3-Dioxygenase-1 is not Critically Involved in Regulating Antitumor Immunity in the Central Nervous System by AP Abu Hejleh, K Huck, K Jähne, CL Tan, TV Lanz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1cc4858be0381cf1c1dd9003a2dfb5aa
Publikováno v:
Science, 2016 May . 352(6289), 1078-1082.
Externí odkaz:
http://www.jstor.org/stable/24748050
Akademický článek
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Publikováno v:
Chemical Communications. 57:10556-10559
A stereoselective, copper-catalyzed, arene C(sp2)–H functionalization/Michael-type annulation reaction involving α-diazocarbonyl compounds has been developed. The method features low catalyst loadings, high yields, and excellent regio and stereose
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c5e8bd83973bfdd44b363e53cdf1248
https://doi.org/10.1039/d1cc04590c
https://doi.org/10.1039/d1cc04590c
Publikováno v:
The Journal of organic chemistry. 86(17)
Studies on Knoevenagel condensations between conjugated dienals and 4-hydroxy-2-pyridone/quinolone-type 1,3-dicarbonyl equivalents led to the development of a simple one-pot strategy to access citridone A and related synthetic cyclopenta[b]furopyrido
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98252cd7b393fcb5d3a5dd066aab19c4
https://pubmed.ncbi.nlm.nih.gov/34410723
https://pubmed.ncbi.nlm.nih.gov/34410723
Publikováno v:
Organic letters. 23(14)
Indolyl α-diazocarbonyl compounds have proven to be effective starting materials for the construction of various 2,3-ring fused indole frameworks. Activation of the diazo functional group under metal catalysis generates a spiro-cyclic indolenine-typ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42c1b7575686ac7c2b13b9a126b76d57
https://pubmed.ncbi.nlm.nih.gov/34197126
https://pubmed.ncbi.nlm.nih.gov/34197126
Publikováno v:
Organic Letters. 22:224-229
The decomposition of diazodicarbonyl compounds in the presence of various metal catalysts has become a reliable method for the functionalization of indoles via carbenoid intermediates. Exploiting t...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ae80cc8be804690161b2483433d4f6a
https://doi.org/10.1021/acs.orglett.9b04210
https://doi.org/10.1021/acs.orglett.9b04210
Autor:
Kenneth Virgel N. Esguerra, Jordan K. Thompson, Danny Q. Thach, Zachary G. Brill, Huck K. Grover, Thomas J. Maimone
Publikováno v:
Angew Chem Int Ed Engl
The ophiobolin sesterterpenes are notable plant pathogens which have recently elicited significant chemical and biological attention because of their intriguing carbogenic frameworks, reactive functionalities, and emerging anticancer profiles. Report
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::572a2507da34953d82a96021aaa671ff
https://doi.org/10.1002/anie.201913150
https://doi.org/10.1002/anie.201913150