Reactivities of stable rotamers. II. Lithiation of 9-(2-methyl-1-naphthyl)-fluorene and related compounds.

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概要

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• Studies were carried out on the rates of lithiation of 9-arylfluorenes, in which the aryls are hydrocarbons. The reactivities of these compounds are explained in terms of the effective blocking of the reaction site by the substituent. The steric effect of the substituent which is attached to the aryl group but is over the fluorene ring is found to play a role in the reactivities.

• 公益社団法人 日本化学会の論文

著者

• Oki Michinori

  Department Of Chemistry Faculty Of Science Okawama University Of Science

• Nakamura Nobuo

  Department Of Cardiology Seiyu Memorial Hospital

• Nakamura Mikio

  Department Of Anatomy Jikei-kai School Of Medicine

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