NMR conformational study reveals that S-C-N anomeric effect in thionucleosides is weaker than O-C-N anomeric effect in natural nucleosides
| Permalink: | http://skupni.nsk.hr/Record/nsk.NSK01000303674/Similar |
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| Matična publikacija: |
Croatica chemica acta 74 (2001), 2 ; str. 381-398 |
| Glavni autor: | Črnugelj, Martin (-) |
| Ostali autori: | Plavec, Janez (-) |
| Vrsta građe: | Članak |
| Jezik: | eng |
| Predmet: |
APA stil citiranja
Črnugelj, M., & Plavec, J. (2001). NMR conformational study reveals that S-C-N anomeric effect in thionucleosides is weaker than O-C-N anomeric effect in natural nucleosides: NMR conformational study reveals that S-C-N anomeric effect in thionucleosides is weaker than O-C-N anomeric effect in natural nucleosides. Croatica chemica acta, p. 4.
Chicago stil citiranjaČrnugelj, Martin, and Janez Plavec. "NMR conformational study reveals that S-C-N anomeric effect in thionucleosides is weaker than O-C-N anomeric effect in natural nucleosides: NMR conformational study reveals that S-C-N anomeric effect in thionucleosides is weaker than O-C-N anomeric effect in natural nucleosides." 2001: 4.
MLA stil citiranjaČrnugelj, Martin, and Janez Plavec. "NMR conformational study reveals that S-C-N anomeric effect in thionucleosides is weaker than O-C-N anomeric effect in natural nucleosides: NMR conformational study reveals that S-C-N anomeric effect in thionucleosides is weaker than O-C-N anomeric effect in natural nucleosides." 2001: 4.