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Collect. Czech. Chem. Commun. 1981, 46, 2540-2556
https://doi.org/10.1135/cccc19812540

Perturbation of the fuchsone chromophore by 3,5-methyl substitution. Sterically crowded exocyclic double bond

Bohumír Kouteka, Lubomír Musila, Jiří Veleka, Antonín Lyčkab, Dobroslav Šnoblb, Miroslava Synáčkováa and Milan Součeka

a Institute of Organic Chemistry and Biochemistry, Czechoslovak Academy of Sciences, 166 10 Prague 6
b Research Institute of Organic Syntheses, 532 18 Pardubice-Rybitví

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  • Taljaard Benjamin, Taljaard Jana H., Imrie Christopher, Caira Mino R.: The Synthesis of Novel p‐Quinone Methides: O‐Dealkylation of5‐(p‐Alkyloxyaryl)‐10,11‐dihydrodibenzo[a,d]cyclohepten‐5‐ols and Related Compounds. Eur J Org Chem 2005, 2005, 2607. <https://doi.org/10.1002/ejoc.200400754>
  • Kurata Hiroyuki, Tanaka Tomomi, Sauchi Toshihiro, Kawase Takeshi, Oda Masaji: Enhanced Nucleophilic Reactivity of a 4-Lithiophenoxide Ion and Its Application to the Synthesis of a Bis(4-hydroxyphenyl)methylenecyclopentadiene and Its Dianion, a Novel Extended Trimethylenemethane Dianion. Chemistry Letters 1997, 26, 947. <https://doi.org/10.1246/cl.1997.947>
  • Benson Mabry, Jurd Leonard: Carbon‐13 NMR of quinone methides. Org. Magn. Reson. 1984, 22, 86. <https://doi.org/10.1002/mrc.1270220206>