Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Mateusz Musiejuk"'
Autor:
Mateusz Musiejuk, Paweł Kafarski
Publikováno v:
Pharmaceuticals, Vol 16, Iss 8, p 1058 (2023)
Lantibiotics are believed to have a conceivable potential to be used as therapeutics, especially against clinically resistant bacterial strains. However, their low solubility and poor stability under physiological conditions limit their availability
Externí odkaz:
https://doaj.org/article/b02b4dc8615245cc81f37f2ce20cade6
Publikováno v:
Journal of the American Chemical Society
Ring-opening of epoxides furnishing either linear or branched products belongs to the group of classic transformations in organic synthesis. However, the regioselective cross-electrophile coupling of aryl epoxides with aryl halides still represents a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4964d1c0f30bcde8b6cb8a88f4a80a0
https://doi.org/10.1021/jacs.1c00659
https://doi.org/10.1021/jacs.1c00659
Autor:
Maria Soledad Marin Navarro, Bartosz Jędrzejewski, Gregorio Ortiz Nieto, Justyna Doroszuk, Mateusz Musiejuk, Dariusz Witt
Publikováno v:
Advanced Synthesis & Catalysis. 362:618-626
We developed a simple and efficient method for the synthesis of functionalized unsymmetrical Z‐alkenyl disulfides under mild conditions in moderate to good yields. The designed method is based on the reaction of α‐thiophosphorylated carbonyl com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cc6980a0476203f95d77516cde0eb230
https://doi.org/10.1002/adsc.201901208
https://doi.org/10.1002/adsc.201901208
Ring-opening of epoxides furnishing either linear or branched products belongs to the group of classic transformations in organic synthesis. However, the regioselective cross-electrophile coupling of aryl epoxides with aryl halides still represents a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e73185dbcbdcb6acfa33785825f1418
https://doi.org/10.26434/chemrxiv.13559852.v1
https://doi.org/10.26434/chemrxiv.13559852.v1
Publikováno v:
European Journal of Organic Chemistry. 2018:6333-6337
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1566dba2272981412433b1a3339c2dc
https://doi.org/10.1002/ejoc.201801181
https://doi.org/10.1002/ejoc.201801181
Publikováno v:
Materials, Vol 14, Iss 1342, p 1342 (2021)
Materials
Materials
The simple, convenient, and efficient methods for the preparation of unsymmetrical vinyl disulfides with additional functional groups under mild conditions with moderate to high yields were designed. The developed methods include the reaction of S-vi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b78e29b169cf7ee6136f8aaf8e4bb946
https://doi.org/10.3390/ma14061342
https://doi.org/10.3390/ma14061342
Autor:
Dariusz Witt, Mateusz Musiejuk
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 191:305-310
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::18f8cf959e03cd4a32bb9f26e7fe6009
https://doi.org/10.1080/10426507.2015.1065258
https://doi.org/10.1080/10426507.2015.1065258
Publikováno v:
RSC Advances. 6:105449-105453
We developed a simple and efficient method for the synthesis of functionalized unsymmetrical alkynyl sulfides under mild conditions in good yields. The designed method is based on the reaction of 5,5-dimethyl-2-thioxo-1,3,2-dioxaphosphorinan-2-disulf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ecc9dcaf97c31defcdab48242fe2e90b
https://doi.org/10.1039/c6ra19440k
https://doi.org/10.1039/c6ra19440k
Autor:
Bartosz Jędrzejewski, Juliusz Maksymilian Walczak, Dariusz Witt, Justyna Doroszuk, Mateusz Musiejuk
Publikováno v:
Materials, Vol 13, Iss 4492, p 4492 (2020)
Materials
Materials
A simple, efficient, and practical sulfenylation at the C2 position of N-tosylindoles under mild conditions was developed. The designed transformation is based on the reaction of N-tosylindoles with BuLi and S-alkyl, and S-aryl phosphorodithioates or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8eaa2987ad647693646856490da99c7a
https://doi.org/10.3390/ma13204492
https://doi.org/10.3390/ma13204492
Publikováno v:
RSC Advances. 5:31347-31351
We developed a simple and efficient method for the synthesis of functionalized unsymmetrical disulfanes under mild conditions in good yields. The designed method is based on the reaction of bis(5,5-dimethyl-2-thioxo-1,3,2-dioxaphosphorinan-2-yl)disul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f44fcc5bb2d1583b15e3a38ea473cbb0
https://doi.org/10.1039/c5ra04173b
https://doi.org/10.1039/c5ra04173b