Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Csongor Hajdu"'
Autor:
Csongor Hajdu
Publikováno v:
Society and Economy. 39:233-250
The opinions of people are expected to forecast their actions, and even major economic institutions rely on this correlation. This research paper examines a case when the opinion of people about their financial situation contradicts their financial-r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f89fae57ccf1b9c502d08e86c2c638d
https://doi.org/10.1556/204.2017.39.2.4
https://doi.org/10.1556/204.2017.39.2.4
Autor:
Csongor Hajdu
Publikováno v:
Corvinus Journal of Sociology and Social Policy. 7:145-150
This paperback version of the Nobel-Prize winning economist Paul Krugman’s New York Times’ best-seller book reviews if the findings in hardcover version remained well-founded after major political and economic actions (US elections, European aust
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbcd4c4bf22bbd65265ffd3b37dfe87d
https://doi.org/10.14267/cjssp.2016.02.10
https://doi.org/10.14267/cjssp.2016.02.10
Autor:
Martin W. G. de Bolster, Henri Stephan Schrekker, Csongor Hajdu, Károly Micskei, Ludger A. Wessjohann, Tamás Patonay
Publikováno v:
Advanced Synthesis & Catalysis. 346:731-736
Ligand induced enantioselective versions of the chromium(II)-mediated Nozaki–Hiyama reaction to homoallyl alcohols proved to be very difficult to achieve, especially if any other nucleophile than the parent allylchromium(III) species was applied. A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e97fdd00777e35ff8b1c849cd1345bf1
https://doi.org/10.1002/adsc.200404021
https://doi.org/10.1002/adsc.200404021
Publikováno v:
ChemInform. 33
A carbon carbon bond forming reaction has been developed by modifying the Nozaki–Hiyama reaction using a chromium(II)-aminopolycarboxylate complexes in a neutral aqueous medium at room temperature. Aldehydes and ketones can be coupled with aralkyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c440baecf392581af63718d82d34c2e
https://doi.org/10.1002/chin.200203068
https://doi.org/10.1002/chin.200203068
Publikováno v:
ChemInform. 37
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::15aaa67d8e8767a9e629e6de54a856d1
https://doi.org/10.1002/chin.200606263
https://doi.org/10.1002/chin.200606263
Autor:
Claudia Zucchi, Valér Marchis, Orsolya Holczknecht, Milena Meo, Tamás Patonay, Gyula Pályi, Károly Micskei, Csongor Hajdu
Stoichiometric reduction of the C,N double bond of oxime precursors of α-amino acids was performed in aqueous media by Cr(II) complexes of natural amino acids. The reduction of oximes of α-ketophenylacetic, α-keto-β-phenylpropionic and α-ketopro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7a324a50ccb5ac167766b739081c28c
Carbon-carbon bond formation in neutral aqueous medium by modification of the Nozaki-Hiyama reaction
A carbon carbon bond forming reaction has been developed by modifying the Nozaki–Hiyama reaction using a chromium(II)-aminopolycarboxylate complexes in a neutral aqueous medium at room temperature. Aldehydes and ketones can be coupled with aralkyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94612c296c09bc76f03694b1044e6aa5
Asymmetric reduction of acetophenone by Cr(II)/amino acid/water/DMF system is reported. Chemical yields up to 94%, enantiomeric excesses up to 74% were observed. The relevance to the Nozaki–Hiyama–Kishi reaction is discussed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::073bf7bcd593f0b76b6303f20cb79f3a
Publikováno v:
Tetrahedron Letters. 40:1373-1374
Prochiral ketones were reduced to enantiomerically enriched secondary alcohols by Cr(II)[L-amino acid] complexes in good yields and moderate enantioselectivity.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed3a54a3f92165775997a3132e7c0d1a
https://doi.org/10.1016/s0040-4039(98)02611-2
https://doi.org/10.1016/s0040-4039(98)02611-2
Autor:
Henri 4;S. Schrekker, Károly Micskei, Csongor Hajdu, Tamás Patonay, Martin 4;W. 4;G. de 4;Bolster, Ludger 4;A. Wessjohann
Publikováno v:
Advanced Synthesis & Catalysis; Jun2004, Vol. 346 Issue 7, p731-736, 6p