Studies on the Meerwein Arylation-Based Preparation of 2, 3-Diarylbenzene-1, 4-diones and Its Theoretical Interpretation.
I Takahashi, O Muramatsu, J Fukuhara, Y Hosokawa…
Index: Takahashi, Ichiro; Muramatsu, Osamu; Fukuhara, Jun; Hosokawa, Yoshinao; Takeyama, Naohiko; et al. Chemistry Letters, 1994 , # 3 p. 465 - 468
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Citation Number: 7
Abstract
466 Chemistry Letters, 1 9 9 4 conformational orientation,6) which is indispensable as the ”hinge” spacer of macrocyclic and open-chain type host molecules.” Based on these findings, the corresponding counterparts, 2,3-diarylbenzene-1,4-diones (4), attract our attention as the candidate of the ”hinge” spacer. In general, synthetic strategies of aryl-substituted benzene-1,4-diones (3-8) in the past can be classified into the following three categories: ...
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