Determination of chemical shifts in 6-condensed syringylic lignin model compounds
Author:
Affiliation:
1. Faculty of Science and Engineering, Åbo Akademi University , Henriksgatan 2 , 20500 Turku/Åbo , Finland
2. Instrument Centre, Åbo Akademi University , Henriksgatan 2 , 20500 Turku/Åbo , Finland
Abstract
Publisher
Walter de Gruyter GmbH
Subject
Biomaterials
Link
https://www.degruyter.com/document/doi/10.1515/hf-2021-0093/pdf
Reference14 articles.
1. Agrawal, P.K. and Thakur, R.S. (1985). 13C NMR spectroscopy of lignan and neolignan derivatives. Magn. Reson. Chem. 23: 389–418, https://doi.org/10.1002/mrc.1260230602.
2. Balakshin, M.Y. and Capanema, E.A. (2015). Comprehensive structural analysis of biorefinery lignins with a quantitative 13C NMR approach. RSC Adv. 5: 87187–87199, https://doi.org/10.1039/c5ra16649g.
3. Balakshin, M., Capanema, E.A., Santos, R.B., Chang, H.M., and Jameel, H. (2016). Structural analysis of hardwood native lignins by quantitative 13C NMR spectroscopy. Holzforschung 70: 95–108, https://doi.org/10.1515/hf-2014-0328.
4. Chen, C.-L. and Robert, D. (1988). Characterization of lignin by 1H and 13C NMR spectroscopy. Methods Enzymol. 161: 137–174, https://doi.org/10.1016/0076-6879(88)61017-2.
5. Gan, L.S., Yang, S.P., Fan, C.Q., and Yue, J.M. (2005). Lignans and their degraded derivatives from Sarcostemma acidum. J. Nat. Prod. 68: 221–225, https://doi.org/10.1021/np049681s.
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