Journal article
Authors list: Fokin, AA; Butkova, ED; Chernish, LV; Fokina, NA; Dahl, JEP; Carlson, RMK; Schreiner, PR
Publication year: 2007
Pages: 2541-2544
Journal: Organic Letters
Volume number: 13
Issue number: 9
ISSN: 1523-7060
DOI Link: https://doi.org/10.1021/ol070920n
Publisher: American Chemical Society
The transformations of apical mono- and bisacetyl diamondoids to the
Abstract:
respective oxetanes and subsequent acid-catalyzed ring
opening/dehydration lead to diamondoidyl mono- and bis-1,3-dienes in
high preparative yields.
Citation Styles
Harvard Citation style: Fokin, A., Butkova, E., Chernish, L., Fokina, N., Dahl, J., Carlson, R., et al. (2007) Simple Preparation of Diamondoid 1,3-Dienes via Oxetane Ring Opening, Organic Letters, 13(9), pp. 2541-2544. https://doi.org/10.1021/ol070920n
APA Citation style: Fokin, A., Butkova, E., Chernish, L., Fokina, N., Dahl, J., Carlson, R., & Schreiner, P. (2007). Simple Preparation of Diamondoid 1,3-Dienes via Oxetane Ring Opening. Organic Letters. 13(9), 2541-2544. https://doi.org/10.1021/ol070920n
