Journalartikel

Simple Preparation of Diamondoid 1,3-Dienes via Oxetane Ring Opening


AutorenlisteFokin, AA; Butkova, ED; Chernish, LV; Fokina, NA; Dahl, JEP; Carlson, RMK; Schreiner, PR

Jahr der Veröffentlichung2007

Seiten2541-2544

ZeitschriftOrganic Letters

Bandnummer13

Heftnummer9

ISSN1523-7060

DOI Linkhttps://doi.org/10.1021/ol070920n

VerlagAmerican Chemical Society


Abstract

The transformations of apical mono- and bisacetyl diamondoids to the
respective oxetanes and subsequent acid-catalyzed ring
opening/dehydration lead to diamondoidyl mono- and bis-1,3-dienes in
high preparative yields.




Zitierstile

Harvard-ZitierstilFokin, 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-ZitierstilFokin, 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



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