Journal article
Authors list: Fokin, AA; Yurchenko, RI; Tkachenko, BA; Fokina, NA; Gunawan, MA; Poinsot, D; Dahl, JEP; Carlson, RMK; Serafin, M; Cattey, H; Hierso, JC; Schreiner, PR
Publication year: 2014
Pages: 5369-5373
Journal: The Journal of Organic Chemistry
Volume number: 79
Issue number: 11
DOI Link: https://doi.org/10.1021/jo500793m
Publisher: American Chemical Society
We present an effective sequence for the preparation of phosphonic acid
Abstract:
derivatives of the diamondoids diamantane, triamantane,
[121]tetramantane, and [1(2,3)4]pentamantane. The reactions of the
corresponding diamondoid hydroxy derivatives with PCl3 in sulfuric or trifluoroacetic acid give mono- as well as didichlorophosphorylated diamondoids in high preparative yields.
Citation Styles
Harvard Citation style: Fokin, A., Yurchenko, R., Tkachenko, B., Fokina, N., Gunawan, M., Poinsot, D., et al. (2014) Selective Preparation of Diamondoid Phosphonates, The Journal of Organic Chemistry, 79(11), pp. 5369-5373. https://doi.org/10.1021/jo500793m
APA Citation style: Fokin, A., Yurchenko, R., Tkachenko, B., Fokina, N., Gunawan, M., Poinsot, D., Dahl, J., Carlson, R., Serafin, M., Cattey, H., Hierso, J., & Schreiner, P. (2014). Selective Preparation of Diamondoid Phosphonates. The Journal of Organic Chemistry. 79(11), 5369-5373. https://doi.org/10.1021/jo500793m
