Crossref Cited-by Linking logo

Collect. Czech. Chem. Commun. 1960, 25, 1492-1499
https://doi.org/10.1135/cccc19601492

On terpenes. CIX. A contribution to the structure of absinthin and anabsinthin

L. Novotný, V. Herout and F. Šorm

Crossref Cited-by Linking

  • Li Chao, Lei Xiaoguang: Strategies toward the Biomimetic Syntheses of Oligomeric Sesquiterpenoids. J. Org. Chem. 2014, 79, 3289. <https://doi.org/10.1021/jo5002092>
  • Malysheva Yulia B., Combes Sebastien, Allegro Diane, Peyrot Vincent, Knochel Paul, Gavryushin Andrei E., Fedorov Alexey Yu.: Synthesis and biological evaluation of novel anticancer bivalent colchicine–tubulizine hybrids. Bioorganic & Medicinal Chemistry 2012, 20, 4271. <https://doi.org/10.1016/j.bmc.2012.05.072>
  • Zhan Zha-Jun, Ying You-Min, Ma Lie-Feng, Shan Wei-Guang: Natural disesquiterpenoids. Nat. Prod. Rep. 2011, 28, 594. <https://doi.org/10.1039/c0np00050g>
  • Schall Andreas, Reiser Oliver: Synthesis of Biologically Active Guaianolides with a trans‐Annulated Lactone Moiety. Eur J Org Chem 2008, 2008, 2353. <https://doi.org/10.1002/ejoc.200700880>
  • Wu Qingquan, Ma Dawei: Recent progress on the total synthesis of natural products in China. Nat. Prod. Rep. 2006, 23, 772. <https://doi.org/10.1039/b609469b>
  • Roth Klaus: Der Zauber der Grünen Fee. Chemie in unserer Zeit 2005, 39, 130. <https://doi.org/10.1002/ciuz.200590014>
  • Zhang Weihe, Luo Shengjun, Fang, Chen Qingshou, Hu Hanwei, Jia Xueshun, Zhai Hongbin: Total Synthesis of Absinthin. J. Am. Chem. Soc. 2005, 127, 18. <https://doi.org/10.1021/ja0439219>
  • Danieli Bruno, Giardini Alessandra, Lesma Giordano, Passarella Daniele, Silvani Alessandra, Appendino Giovanni, Noncovich Alain, Fontana Gabriele, Bombardelli Ezio, Sterner Olov: Synthesis and Biological Evaluation of PaclitaxelThiocolchicine Hybrids. Chemistry & Biodiversity 2004, 1, 327. <https://doi.org/10.1002/cbdv.200490029>
  • Belitz Hans‐Dieter, Wieser Herbert: Bitter compounds: Occurrence and structure‐activity relationships. Food Reviews International 1985, 1, 271. <https://doi.org/10.1080/87559128509540773>
  • Kasymov Sh. Z.: Advances in the chemistry of sesquiterpene lactones. Chem Nat Compd 1982, 18, 519. <https://doi.org/10.1007/BF00575031>
  • Seaman Frederick C.: Sesquiterpene lactones as taxonomic characters in the asteraceae. Bot. Rev 1982, 48, 121. <https://doi.org/10.1007/BF02919190>
  • Beauhaire J., Fourrey J.L., Lallemand J.Y., Vullhorgne M.: Dimeric sesquiterpene lactone. Structure of isoabsinthin acid isomerization of absinthin derivatives. Tetrahedron Letters 1981, 22, 2269. <https://doi.org/10.1016/S0040-4039(01)92907-7>
  • Beauhaire J., Fourrey J.L., Vuilhorgne M., Lallemand J.Y.: Dimeric sesquiterpene lactones : Structure of absinthin. Tetrahedron Letters 1980, 21, 3191. <https://doi.org/10.1016/S0040-4039(00)77442-9>
  • Kasymov Sh. Z., Abdullaev N. D., Sidyakin G. P., Yagudaev M. R.: Anabsin — A new diguaianolide fromArtemisia absinthium. Chem Nat Compd 1979, 15, 430. <https://doi.org/10.1007/BF00565040>
  • Zakirov S. Kh., Kasymov Sh. Z., Sidyakin G. P.: Structures of ashurbin and arabsin. Chem Nat Compd 1976, 12, 492. <https://doi.org/10.1007/BF00564834>
  • Vokáč K., Samek Z., Herout V., S̆orm F.: The Structure of Artabsin and Absinthin. Tetrahedron Letters 1968, 9, 3855. <https://doi.org/10.1016/S0040-4039(01)99119-1>
  • Steelink Cornelius, Spitzer Jeffrey C.: Sesquiterpene lactones in chemotaxonomy. Phytochemistry 1966, 5, 357. <https://doi.org/10.1016/S0031-9422(00)82149-4>
  • Schwär Christine: Die Wirkung isolierter Wermutinhaltsstoffe auf Foeniculum vulgare Mill., Lepidium sativum L. und Lactuca sativa L. var. longifolia Lam. Flora oder Allgemeine Botanische Zeitung 1962, 152, 509. <https://doi.org/10.1016/S0367-1615(17)32611-3>