Monoterpene syntheses via a palladium catalyzed isoprene dimerization
作者:James P. Neilan、Richard M. Laine、Nicholas Cortese、Richard F. Heck
DOI:10.1021/jo00883a030
日期:1976.10
A Study of Organic Parachors. IX. The Additive Nature of Structural Units in the Parachors of Ditertiary Glycols and Chlorides<sup>1,2</sup>
作者:Thomas P. Johnston、Osborne R. Quayle
DOI:10.1021/ja01182a012
日期:1948.2
Bouvet, Bulletin de la Societe Chimique de France, 1915, vol. <4> 17, p. 215
作者:Bouvet
DOI:——
日期:——
The Development of Synthetic Routes to 1,1,<i>n</i>,<i>n</i>-Tetramethyl[<i>n</i>](2,11)teropyrenophanes
作者:Kiran Sagar Unikela、Bradley L. Merner、Parisa Ghods Ghasemabadi、C. Chad Warford、Christopher S. Qiu、Louise N. Dawe、Yuming Zhao、Graham J. Bodwell
DOI:10.1002/ejoc.201900707
日期:2019.7.31
BIG BEND chimes in – this is not second hand news! Every minute detail of the synthesis of a striking series of 1,1,n,n‐tetramethyl[n](2,11)teropyrenophanes (n=7–9) is described. The end‐to‐end bend in the teropyrene system clocks in at as much as 177.9°.
大弯曲声响起–这不是二手新闻!详细介绍了惊人的1,1, n, n-四甲基[ n ](2,11)萜烯基庚烯( n = 7–9)系列的合成。萜品system体系的端对端弯曲时脉可达177.9°。