Crossref Cited-by Linking logo

Collect. Czech. Chem. Commun. 1980, 45, 330-334
https://doi.org/10.1135/cccc19800330

Analysis of 1H-NMR spectra of cinnamaldehyde type model substances of lignin

Tibor Liptaja, Milan Remkob and Ján Polčinc

a Central NMR Laboratory, Slovak Institute of Technology, 880 37 Bratislava
b Scientific Research Institute of Pharmaceutical Faculty, Comenius University, 880 34 Bratislava
c Pulp and Paper Research Institute, 890 20 Bratislava

Crossref Cited-by Linking

  • Mokoena Terrinne P., Maluleka Marole M., Mampa Richard M., Mphahlele Malose J., Monchusi Bernice A.: Synthesis, crystal structures, spectroscopic characterization and in vitro evaluation of the 4-sulfono-3-methoxycinnamaldehydes as potential α-glucosidase and/or α-amylase inhibitors. Journal of Molecular Structure 2023, 1271, 134119. <https://doi.org/10.1016/j.molstruc.2022.134119>
  • Brillatz Théo, Kubo Miwa, Takahashi Shimon, Jozukuri Natsumi, Takechi Kenshi, Queiroz Emerson Ferreira, Marcourt Laurence, Allard Pierre-Marie, Fish Richard, Harada Kenichi, Ishizawa Keisuke, Crawford Alexander D., Fukuyama Yoshiyasu, Wolfender Jean-Luc: Metabolite Profiling of Javanese Ginger Zingiber purpureum and Identification of Antiseizure Metabolites via a Low-Cost Open-Source Zebrafish Bioassay-Guided Isolation. J. Agric. Food Chem. 2020, 68, 7904. <https://doi.org/10.1021/acs.jafc.0c02641>
  • Liang Shuang, Shen Yun-Heng, Tian Jun-Mian, Wu Zhi-Jun, Jin Hui-Zi, Zhang Wei-Dong, Yan Shi-Kai: Phenylpropanoids from Daphne feddei and Their Inhibitory Activities against NO Production. J. Nat. Prod. 2008, 71, 1902. <https://doi.org/10.1021/np8004166>
  • Xie Wei-Dong, Zhang Qi, Li Ping-Lin, Jia Zhong-Jian: Two triterpenoids and other constituents from Petasites tricholobus. Phytochemistry 2005, 66, 2340. <https://doi.org/10.1016/j.phytochem.2005.03.032>
  • Sarker Satyajit D, Bartholomew Barbara, Nash Robert J, Simmonds Monique S.J: Sideroxylin and 8-demethylsideroxylin from Eucalyptus saligna (Myrtaceae). Biochemical Systematics and Ecology 2001, 29, 759. <https://doi.org/10.1016/S0305-1978(00)00108-3>
  • Sun Rongqi, Sacalis John N., Chin Chee-Kok, Still Cecil C.: Bioactive Aromatic Compounds from Leaves and Stems of Vanilla fragrans. J. Agric. Food Chem. 2001, 49, 5161. <https://doi.org/10.1021/jf010425k>
  • Banskota Arjun H., Tezuka Yasuhiro, Prasain Jeevan K., Matsushige Katsumichi, Saiki Ikuo, Kadota Shigetoshi: Chemical Constituents of Brazilian Propolis and Their Cytotoxic Activities. J. Nat. Prod. 1998, 61, 896. <https://doi.org/10.1021/np980028c>
  • Bízik Frantisek, Tvaroska Igor, Remko Milan: Conformational analysis of ester and ether linkages in lignin-arabinoxylan complexes. Carbohydrate Research 1994, 261, 91. <https://doi.org/10.1016/0008-6215(94)80008-1>
  • Keiko N. A., Rulev A. Yu., Kalikhman I. D., Voronkov M. G.: Structure of N,N-disubstituted ?,?-unsaturated ?-amino aldehydes. Russ Chem Bull 1991, 40, 1796. <https://doi.org/10.1007/BF00960405>
  • T�nnesen Hanne Hjorth, Karlsen Jan, Henegouwen Gerard Beijersbergen: Studies on curcumin and curcuminoids VIII. Photochemical stability of curcumin. Z Lebensm Unters Forch 1986, 183, 116. <https://doi.org/10.1007/BF01041928>
  • Unterhalt Bernard, Eljabour Sulaiman, Weyrich Klaus: Notiz zur Darstellung substituierter Zimtaldehyde The Synthesis of Substituted Cinnamyl Aldehydes. Archiv der Pharmazie 1983, 316, 574. <https://doi.org/10.1002/ardp.19833160619>
  • Remko Milan, Sekerka Ivan: MO Investigations on Lignin Model Compounds. Zeitschrift für Physikalische Chemie 1983, 134, 135. <https://doi.org/10.1524/zpch.1983.134.2.135>