Crossref Cited-by Linking logo

Collect. Czech. Chem. Commun. 1954, 19, 1205-1214
https://doi.org/10.1135/cccc19541205

Über die Dimerisierung des α-Angelicalactons

R. Lukeš and K. Syhora

Crossref Cited-by Linking

  • Mascal Mark, Dutta Saikat, Gandarias Inaki: Hydrodeoxygenation of the Angelica Lactone Dimer, a Cellulose‐Based Feedstock: Simple, High‐Yield Synthesis of Branched C7–C10 Gasoline‐like Hydrocarbons. Angewandte Chemie 2014, 126, 1885. <https://doi.org/10.1002/ange.201308143>
  • Mascal Mark, Dutta Saikat, Gandarias Inaki: Hydrodeoxygenation of the Angelica Lactone Dimer, a Cellulose‐Based Feedstock: Simple, High‐Yield Synthesis of Branched C7–C10 Gasoline‐like Hydrocarbons. Angew Chem Int Ed 2014, 53, 1854. <https://doi.org/10.1002/anie.201308143>
  • Xin Jiayu, Zhang Suojiang, Yan Dongxia, Ayodele Olubunmi, Lu Xingmei, Wang Jianji: Formation of C–C bonds for the production of bio-alkanes under mild conditions. Green Chem. 2014, 16, 3589. <https://doi.org/10.1039/C4GC00501E>
  • Ueda Mitsuru, Yabuuchi Masahiko, Imai Yoshio: Synthesis of polyamides by ring‐opening polyaddition of 4,4′‐disubstituted bis(3‐buten‐4‐olide) with aliphatic diamines. J. Polym. Sci. Polym. Chem. Ed. 1977, 15, 73. <https://doi.org/10.1002/pol.1977.170150108>
  • Ficini Jacqueline, d'Angelo Jean, Genêt Jean-Pierre, Noiré Jeannine: Synthèse de la dihydrojasmone et de la cis jasmone, à partir de l'angélicalactone. Tetrahedron Letters 1971, 12, 1569. <https://doi.org/10.1016/S0040-4039(01)97012-1>