| Literature DB >> 16671765 |
Tsuyoshi Sawada1, Yousuke Nishiyama, Wataru Tabuchi, Makoto Ishikawa, Emi Tsutsumi, Yutaka Kuwahara, Hideto Shosenji.
Abstract
[reaction: see text] Tetramethoxy[2.1.2.1]metacyclophane ([2.1.2.1]MCP) was prepared by the pinacol coupling reaction of diphenylmethane dialdehyde. The treatment of [2.1.2.1]MCP with trimethylsilyl chloride and sodium iodide yielded two unexpected calixarene derivatives, cone (hemisphere) and 1,2-alternate types, instead of octahydroxy[2.1.2.1]MCP. The X-ray structure of the cone-type derivative and its inclusion property with acetonitrile were also discussed.Entities:
Year: 2006 PMID: 16671765 DOI: 10.1021/ol060286y
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005