Fluorination of some highly functionalized cycloalkanes chemoselectivity and substrate dependence /
A study exploring the chemical behavior of some dihydroxylated beta-amino ester stereo-and regioisomers, derived from unsaturated cyclic beta-amino acids is described. The nucleophilic fluorinations involving hydroxy-fluorine exchange of some highly functionalized alicyclic diol derivatives have bee...
Elmentve itt :
Szerzők: | |
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Dokumentumtípus: | Cikk |
Megjelent: |
2017
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Sorozat: | BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY
13 |
Tárgyszavak: | |
doi: | 10.3762/bjoc.13.233 |
mtmt: | 3296049 |
Online Access: | http://publicatio.bibl.u-szeged.hu/12508 |
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490 | 0 | |a BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY |v 13 | |
520 | 3 | |a A study exploring the chemical behavior of some dihydroxylated beta-amino ester stereo-and regioisomers, derived from unsaturated cyclic beta-amino acids is described. The nucleophilic fluorinations involving hydroxy-fluorine exchange of some highly functionalized alicyclic diol derivatives have been carried out in view of selective fluorination, investigating substrate dependence, neighboring group assistance and chemodifferentiation. | |
650 | 4 | |a Általános orvostudomány | |
700 | 0 | 1 | |a Nonn Melinda |e aut |
700 | 0 | 1 | |a Fustero Santos |e aut |
700 | 0 | 1 | |a Haukka Matti |e aut |
700 | 0 | 1 | |a Fülöp Ferenc |e aut |
700 | 0 | 1 | |a Kiss Loránd |e aut |
856 | 4 | 0 | |u http://publicatio.bibl.u-szeged.hu/12508/1/remete_beilstein.pdf |z Dokumentum-elérés |