Crossref Cited-by Linking logo

Collect. Czech. Chem. Commun. 1964, 29, 516-530
https://doi.org/10.1135/cccc19640516

Nebenprodukte bei der Umsetzung von Allobetulin zu Heterobetulin

J. Klinot and A. Vystrčil

Crossref Cited-by Linking

  • Arrous Salah, Boudebouz Imene, Bakibaev Abdigali, Hoang Phuoc, Parunov I.: Novel Method for O-Acetylation of Cholesterol, Allobetulin, and Betulin. Chem Nat Compd 2019, 55, 482. <https://doi.org/10.1007/s10600-019-02720-9>
  • Tolmacheva Irina A., Nazarov Alexey V., Dmitriev Maxim V., Boreko Eugene I., Grishko Victoria V.: Synthesis of 1,10-seco-triterpenoids by the Beckmann fragmentation from allobetulin. Tetrahedron 2017, 73, 6448. <https://doi.org/10.1016/j.tet.2017.09.044>
  • Khusnutdinova El’mira F., Medvedeva Natalya I., Kazakov Dmitri V., Kukovinets Olga S., Lobov Alexander N., Suponitsky Kirill Yu., Kazakova Oxana B.: An efficient synthesis of moronic and heterobetulonic acids from allobetulin. Tetrahedron Letters 2016, 57, 148. <https://doi.org/10.1016/j.tetlet.2015.11.086>
  • Kazakova O. B., Khusnutdinova É. F., Medvedeva N. I., Lobov A. N., Suponitskii K. Yu.: Molecular structure of 1,2,6,6,10,16,17-heptamethyl-20-(acetoxymethyl)pentacyclo [12.8.0.02.11.05.10.015.20]docos-17-en-7-yl acetate. J Struct Chem 2012, 53, 954. <https://doi.org/10.1134/S0022476612050198>
  • Dehaen Wim, Mashentseva Anastassiya A., Seitembetov Talgat S.: Allobetulin and Its Derivatives: Synthesis and Biological Activity. Molecules 2011, 16, 2443. <https://doi.org/10.3390/molecules16032443>
  • Salvador Jorge A. R., Pinto Rui M. A., Santos Rita C., Le Roux Christophe, Beja Ana Matos, Paixão José A.: Bismuth triflate-catalyzed Wagner-Meerwein rearrangement in terpenes. Application to the synthesis of the 18α-oleanane core and A-neo-18α-oleanene compounds from lupanes. Org. Biomol. Chem. 2009, 7, 508. <https://doi.org/10.1039/B814448F>
  • Huneck Siegfried: Photochemische Umsetzungen, IV; Triterpene, XII: Die Darstellung von 19β.28-Epoxy-1-oxo-2-diazo-18αH-oleanan und dessen photochemische und thermische Umwandlung in A-Nor-Verbindungen. Chem. Ber. 1965, 98, 2291. <https://doi.org/10.1002/cber.19650980731>