Journal article
Authors list: Fokin, AA; Butova, ED; Barabash, AV; Huu, NH; Tkachenko, BA; Fokina, NA; Schreiner, PR
Publication year: 2013
Pages: 1772-1777
Journal: Synthetic Communications
Volume number: 43
Issue number: 13
ISSN: 0039-7911
DOI Link: https://doi.org/10.1080/00397911.2012.667491
Publisher: Taylor and Francis Group
We describe a convenient four-step preparation of 1- vinyl adamantane,
Abstract:
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.
Citation Styles
Harvard Citation style: Fokin, A., Butova, E., Barabash, A., Huu, N., Tkachenko, B., Fokina, N., et al. (2013) Preparative Synthesis of Vinyl Diamondoids, Synthetic Communications, 43(13), pp. 1772-1777. https://doi.org/10.1080/00397911.2012.667491
APA Citation style: Fokin, A., Butova, E., Barabash, A., Huu, N., Tkachenko, B., Fokina, N., & Schreiner, P. (2013). Preparative Synthesis of Vinyl Diamondoids. Synthetic Communications. 43(13), 1772-1777. https://doi.org/10.1080/00397911.2012.667491