Synthesis and Diatropicity of a Phenanthrene-Annelated trans-Dimethyldihydropyrene: A Novel Molecule To Indicate the High ?-Bond Order of the 9,10 bond of Phenanthrene

DOI: 10.1021/ja00309a042

Source and publish data:

Journal of the American Chemical Society p. 6678 - 6683 (1985)

Update date:2022-08-04

Topics:: Authors:

Lai, Yee-Hing

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Article abstract of DOI:10.1021/ja00309a042

The trans-phenanthrodimethyldihydropyrene 6 has been synthesized from phenanthraquinone and 2,6-dichlorotoluene in 0.3-0.5percent overall yield by using Stevens or Wittig rearrangements and a Hofmann elimination sequence on the thiacyclophane 8B followed

Full text of DOI:10.1021/ja00309a042

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Article Doi

Synthesis and Diatropicity of a Phenanthrene-Annelated trans-Dimethyldihydropyrene: A Novel Molecule To Indicate the High ?-Bond Order of the 9,10 bond of Phenanthrene

DOI: 10.1021/ja00309a042

Source and publish data:

Authors:

Article abstract of DOI:10.1021/ja00309a042

Full text of DOI:10.1021/ja00309a042

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