We describe a convenient four-step preparation of 1- vinyl adamantane, 1- vinyl diamantane, and 4,9-divinyl diamantane from the respective diamondoid acetic acids in 50-80% isolated yields involving esterification, reduction, and hydrobromination/dehydrobromination.Supplemental materials are available for this article. Go to the publisher's online edition of Synthetic Communications (R) to view the free supplemental file.
作者:Andrey A. Fokin、Ekaterina D. Butova、Anastasiya V. Barabash、Nhan N. Huu、Boryslav A. Tkachenko、Natalie A. Fokina、Peter R. Schreiner
DOI:10.1080/00397911.2012.667491
日期:2013.7.3
We describe a convenient four-step preparation of 1- vinyl adamantane, 1- vinyl diamantane, and 4,9-divinyl diamantane from the respective diamondoid acetic acids in 50-80% isolated yields involving esterification, reduction, and hydrobromination/dehydrobromination.Supplemental materials are available for this article. Go to the publisher's online edition of Synthetic Communications (R) to view the free supplemental file.
VODICHKA, L.;BURKXARD, I.;ZAXARZH, I.;ISAEV, S. D.;SAJCHENKO, S. I.;YURCH+, ZH. ORGAN. XIMII, 1985, 21, N 12, 2569-2574
作者:VODICHKA, L.、BURKXARD, I.、ZAXARZH, I.、ISAEV, S. D.、SAJCHENKO, S. I.、YURCH+