Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Svatava Voltrová"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 17, Iss 1, Pp 2657-2662 (2021)
The stereoselective Suzuki–Miyaura cross-coupling of (Z)-β-enamido triflates is demonstrated. Depending on the nature of the ligand in the palladium catalyst, either retention or inversion of the configuration during the synthesis of β,β-diaryl-
Externí odkaz:
https://doaj.org/article/7b94af38547547c9bdfa90569580cc54
Autor:
Anna Kubíčková, Athanasios Markos, Svatava Voltrová, Anežka Marková, Josef Filgas, Blanka Klepetářová, Petr Slavíček, Petr Beier
Publikováno v:
Organic Chemistry Frontiers.
N-Fluoroalkylated 1,2,3-triazoles underwent a microwave-heating-assisted ring opening, nitrogen molecule elimination and concomitant group rearrangement to form isolable N-fluoroalkylketenimines.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4890154b456267035b72e64017869da1
https://doi.org/10.1039/d3qo00618b
https://doi.org/10.1039/d3qo00618b
Autor:
Zsófia E. Blastik, Svatava Voltrová, Václav Matoušek, Bronislav Jurásek, David W. Manley, Blanka Klepetářová, Petr Beier
Publikováno v:
Angewandte Chemie. 129:352-355
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7ac6adf2679c57b70da27d0e6e9f24f0
https://doi.org/10.1002/ange.201609715
https://doi.org/10.1002/ange.201609715
Autor:
Svatava Voltrová
Publikováno v:
Fluorine Notes. 115:2-2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd2816fa9ed1352513baa7f23a9027b1
https://doi.org/10.17677/fn20714807.2017.06.02
https://doi.org/10.17677/fn20714807.2017.06.02
Autor:
Viktor Prutianov, Svatava Voltrová
Publikováno v:
Molecules. 1:207-211
1-Oxides of 4-nitro-3-pyridinecarboxylic acid (3) and methyl 4-methoxy-3-pyridinecarboxylate (5) were converted to 4-(diphenylmethyl)amino (7), 4-phenylthio (8), 4-phenylamino (9) and 4-(2-methylpropyl)-amino (6) derivatives by reaction with the corr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2cc4a563018df0b50d4f184315a1488
https://doi.org/10.1007/s007830050039
https://doi.org/10.1007/s007830050039
Publikováno v:
ChemInform. 28
3-Hydroxymethyl-5-(2,3- O -isopropylidene-β-D- erythro- furanosyl)-2-methylfuran ( 2 ) prepared from 3-ethoxycarbonyl derivative 1 was converted to 3-chloromethyl-5-(2,3- O -isopropylidene-β-D- erythro -furanosyl)-2-methylfuran ( 3 ). Compound 3 re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6fa875e3861a1a1c8150adafcc23e8a7
https://doi.org/10.1002/chin.199709189
https://doi.org/10.1002/chin.199709189