## Abstract The ^1^H and ^13^C NMR spectra of ‘Thiele's ester,’ i.e. dimethyl 3α 4α, 7α, 7α‐tetrahydro‐4,7‐methano‐1H‐indene‐2,6‐dicarboxylate, have been assigned completely by using a combination of one‐ and two‐dimensional NMR techniques. The results thereby obtained afford the first unambiguous
Complete assignment of the NMR spectra of [D-Leu1]-microcystin-LR and analysis of its solution structure
✍ Scribed by Jan Schripsema; Denise Dagnino
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 99 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.1059
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✦ Synopsis
Abstract
[D‐Leu^1^]‐microcystin‐LR is a recently discovered microcystin. We report the isolation of this microcystin analogue from a Microcystis aeruginosa strain isolated from the Lagoa de Iquipari, Rio de Janeiro, Brazil. The ^1^H and ^13^C NMR spectra were completely assigned in both MeOH‐d~4~ and DMSO‐d~6~. Further, the solution structure of this compound was investigated with the use of two‐dimensional NMR and the amide proton temperature dependence, and was compared with those of its analogs, microcystin‐RR and microcystin‐LR. Copyright © 2002 John Wiley & Sons, Ltd.
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