| Literature DB >> 16881630 |
Toshiyuki Hamura1, Yousuke Ibusuki, Hidehiro Uekusa, Takashi Matsumoto, Jay S Siegel, Kim K Baldridge, Keisuke Suzuki.
Abstract
We report herein the syntheses of dodecamethoxytricyclobutabenzene (TCBB) 1 and hexaoxo-TCBB 2, a class of molecules with structural and theoretical interest. The preparation is based on the 3-fold [2 + 2] cycloadditions of benzyne and ketene silyl acetals (KSAs), where the selectively protected 2-iodophloroglucinol derivative served as a synthetic equivalent of benztriyne I, allowing rapid and regioselective annulation of fully functionalized four-membered rings. Structural study on the former compound showed that the C-C bond lengths in the central benzene ring were essentially the same.Entities:
Year: 2006 PMID: 16881630 DOI: 10.1021/ja064063e
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419