Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Michał, Karchier"'
Autor:
Marek Masnyk, Patrycja Ruśkowska, Beata Słomińska, Jadwiga Frelek, Marcin Górecki, Jarosław Jaźwiński, Michał Karchier, Agata Suszczyńska, Magdalena Jawiczuk, Przemysław Kalicki
Publikováno v:
ResearcherID
Full characterization of the adduct isolated in crystalline form from a solution of tetrakis (μ-trifluoroacetato) dimolybdenum(II) and (2 S ,3 S )-butane-2,3-diol is reported herein. For this purpose X-ray crystallographic, spectroscopic, and comput
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e506e5171a588b34fbea5a2be94fae8c
https://doi.org/10.1016/j.tetasy.2014.10.008
https://doi.org/10.1016/j.tetasy.2014.10.008
Publikováno v:
Chirality. 26:300-306
A series of representative optically active derivatives of 4-hydroxy-5-alkylcyclopent-2-en-1-one were prepared from the respective 2-furyl methyl carbinols via the Piancatelli rearrangement followed by the enzymatic kinetic resolution of racemates. A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8a6005af659f1fb8711105a579e7883
https://doi.org/10.1002/chir.22322
https://doi.org/10.1002/chir.22322
Autor:
Jarosław Jaźwiński, Magdalena Jawiczuk, Jadwiga Frelek, Marcin Górecki, Michał Karchier, Agata Suszczyńska
Publikováno v:
Inorganic Chemistry. 52:8250-8263
The aim of the present work was to check the suitability of dimolybdenum carboxylates, other than commonly used [Mo2(OAc)4], as auxiliary chromophores for determining the absolute configuration of optically active vic-diols by means of electronic cir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::721ee63e8d515438cfceaa88a92128e6
https://doi.org/10.1021/ic401170m
https://doi.org/10.1021/ic401170m
Autor:
Jadwiga, Frelek, Michał, Karchier, Daria, Madej, Karol, Michalak, Paweł, Różański, Jerzy, Wicha
Publikováno v:
Chirality. 26(6)
A series of representative optically active derivatives of 4-hydroxy-5-alkylcyclopent-2-en-1-one were prepared from the respective 2-furyl methyl carbinols via the Piancatelli rearrangement followed by the enzymatic kinetic resolution of racemates. A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5560e3fe20c4ec36daf77a7830eea20b
https://pubmed.ncbi.nlm.nih.gov/24788690
https://pubmed.ncbi.nlm.nih.gov/24788690
Publikováno v:
ChemInform. 41
Treatment of 2,3-epoxy alcohols of type (I), (V), and (VIII) with Cl-CS-NMe2 results in formation of the corresponding thiocarbamate derivatives which are unstable and undergo rearrangement to 2,3-epithio alcohol derivatives at room temperature.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4fe8e5c6f0ffec028f455d5832ef84ee
https://doi.org/10.1002/chin.201050096
https://doi.org/10.1002/chin.201050096
Publikováno v:
The Journal of organic chemistry. 75(15)
Transformation of representative 2,3-epoxy alcohols, including 3-trimethylsilyl- and 3-triphenylsilylglycidols, into the corresponding 2,3-epithio alcohol dimethylthiocarbamate derivatives under mild alkaline conditions is reported.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d004d6c2ec1c47469710a86f7386a668
https://pubmed.ncbi.nlm.nih.gov/20670038
https://pubmed.ncbi.nlm.nih.gov/20670038