Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Eva Solčániová"'
Publikováno v:
ARKIVOC, Vol 2005, Iss 5, Pp 103-115 (2005)
Externí odkaz:
https://doaj.org/article/28902ec2374244a795fcc4aa563b8402
Autor:
Zuzana Čurillová, Peter Kutschy, Eva Solčániová, Martina Pilátová, Ján Mojžiš, and Vladimír Kováčik
Publikováno v:
ARKIVOC, Vol 2008, Iss 8, Pp 85-104 (2008)
Externí odkaz:
https://doaj.org/article/6813a96d72864b12958a995592a1a91c
Autor:
Martin Humenik, Vladimír Kováčik, Slávka Bekešová, Eva Solčániová, Peter Kutschy, Milan Dzurilla
Publikováno v:
Collection of Czechoslovak Chemical Communications. 69:1657-1674
The linear synthesis of 1-(β-D-glucopyranosyl)-, 1-(β-D-galactopyranosyl)-, 1-(β-D-mannopyranosyl)- and 1-(β-D-ribofuranosyl)benzocamalexin was elaborated from indoline as a starting compound and corresponding pentaacetylhexoses or 1-O-acetyl-2,3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f7579535f4cab1eba62a8dbcbb4e80a
https://doi.org/10.1135/cccc20041657
https://doi.org/10.1135/cccc20041657
Publikováno v:
Journal of Organometallic Chemistry. 659:43-49
The diastereoselectivity of [3+2] cycloaddition of tricarbonyl[(4,5,6,7-η)-2-methyltropone]iron (2) with an E,Z isomeric mixture of η1-(crotyl)Fp (4E/4Z) [Fp: C5H5Fe(CO)2 or CpFe(CO)2] has been studied. By this cyclopentaanulation, four stereogenic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::22f860c33a9cb39b7829126deb37c497
https://doi.org/10.1016/s0022-328x(02)01671-6
https://doi.org/10.1016/s0022-328x(02)01671-6
Publikováno v:
Green Chemistry. 4:103-106
Enantioselective Pd-catalyzed allylic substitution of (rac)-(E)-1,3-diphenyl-3-acetoxyprop-1-ene with dimethyl malonate was studied in 3-butyl-1-methylimidazolium hexafluorophosphate ([bmim][PF6]) as an ionic liquid. The reactions were catalyzed by P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ed1942e68c299c66311206949364507
https://doi.org/10.1039/b109178f
https://doi.org/10.1039/b109178f
Novel Chiral 1-(ferrocenylalkyl)-( S )-prolinols and their Application in Enantioselective Synthesis
Publikováno v:
Tetrahedron. 56:671-675
Diastereomeric ferrocenylphosphine ligands, (−)-( S , R , pS )-BPPF-Pro ( 3a ) and (+)-( S , S , pR )-BPPF-Pro ( 3b ), containing the ( S )-prolinol moiety were prepared. A detailed structural elucidation of these ligands was carried out using NMR.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::535b9650a5b21f478528ccefe61f6afc
https://doi.org/10.1016/s0040-4020(99)01040-6
https://doi.org/10.1016/s0040-4020(99)01040-6
Publikováno v:
Collection of Czechoslovak Chemical Communications. 64:99-106
Acetylations of 3-ferrocenyl-1-methylpyrrole as well as 3-cyano-4-ferrocenylpyrrole and 3-cyano-4-ferrocenyl-1-methylpyrrole were performed. The course of the acylation is highly dependent on the acylation agent, that is acetyl chloride/aluminum chlo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6f9f8fa3eb97f816d363a2b1288a9425
https://doi.org/10.1135/cccc19990099
https://doi.org/10.1135/cccc19990099
Autor:
Štefan Toma, and Ali A. Torabi, Eva Solčániová, Kenneth W. Muir, Graham R. Knox, Monika Prokešová
Publikováno v:
The Journal of Organic Chemistry. 61:3392-3397
The Diels−Alder reactions of 1,3-diphenylisobenzofuran with acryloylferrocene (1), 4-ferrocenyl-3-buten-2-one (2), cinnamoylferrocene (3), 3-ferrocenyl-1-phenyl-2-propenone (4), chalcone (5), 1-((η6-phenyl)tricarbonylchromio)-3-phenyl-2-propenone
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::25ff6c5c06145aec25c431ab2c07782e
https://doi.org/10.1021/jo9500850
https://doi.org/10.1021/jo9500850
Publikováno v:
Tetrahedron. 50:5765-5774
Friedel-Crafts acetylation, Vilsmeier-Haack formylation and BuLi metallation followed by DMF quenching of 2-ferrocenylthiophene, 2-ferrocenyl-3-phenylthiophene, 2-ferrocenyl-5-phenylthiophene, 2-ferrocenyl-1-methylpyrrole and 2-ferrocenyl-1-methyl-3-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dcc89f6a01527c756e3f2fcd3643d968
https://doi.org/10.1016/s0040-4020(01)85644-1
https://doi.org/10.1016/s0040-4020(01)85644-1
Publikováno v:
Collection of Czechoslovak Chemical Communications. 58:2128-2138
Michael addition of C-nucleophiles to 2-benzylidine[3]ferrocenophane-1,3-dione has been studied. In some cases, (ethyl acetoacetate, acetylacetone and malononitrile as the C-nucleophiles) the addition was followed by intramolecular cyclization leadin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a47fdcfbfbe3e50a247b87915ec75e42
https://doi.org/10.1135/cccc19932128
https://doi.org/10.1135/cccc19932128