Collect. Czech. Chem. Commun.
1997, 62, 1747-1753
https://doi.org/10.1135/cccc19971747
Gradient-Enhanced Inverse-Detected NMR Techniquesfor Determination of 1H-15N Coupling Constants in 2,2-Dimethylpenta-3,4-dienal Derivatives
Radek Marek
NMR Laboratory, Masaryk University, Kotlářská 2, 611 37 Brno, Czech Republic
Crossref Cited-by Linking
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- Marek Radek, Humpa Otakar, Dostál Jiří, Slavík Jiří, Sklenář Vladimír: 15N NMR study of isoquinoline alkaloids. Magn Reson Chem 1999, 37, 195. <https://doi.org/10.1002/(SICI)1097-458X(199903)37:3<195::AID-MRC435>3.0.CO;2-D>
- Marek Radek, Humpa Otakar, Dostál Jiří, Slavík Jiří, Sklenář Vladimír: 15N NMR study of isoquinoline alkaloids. Magn. Reson. Chem. 1999, 37, 195. <https://doi.org/10.1002/(SICI)1097-458X(199903)37:3<195::AID-MRC435>3.0.CO;2-D>
- Hocková Dana, Buděšínský Miloš, Marek Radek, Marek Jaromír, Holý Antonín: Regioselective Preparation ofN7- andN9-Alkyl Derivatives ofN6-[(Dimethylamino)methylene]adenine Bearing an Active Methylene Group and Their Further Derivatization Leading to α-Branched Acyclic Nucleoside Analogues. Eur J Org Chem 1999, 1999, 2675. <https://doi.org/10.1002/(SICI)1099-0690(199910)1999:10<2675::AID-EJOC2675>3.0.CO;2-Z>
- Hocková Dana, Buděšínský Miloš, Marek Radek, Marek Jaromír, Holý Antonín: Regioselective Preparation ofN7- andN9-Alkyl Derivatives ofN6-[(Dimethylamino)methylene]adenine Bearing an Active Methylene Group and Their Further Derivatization Leading to α-Branched Acyclic Nucleoside Analogues. Eur. J. Org. Chem. 1999, 1999, 2675. <https://doi.org/10.1002/(SICI)1099-0690(199910)1999:10<2675::AID-EJOC2675>3.0.CO;2-Z>
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