Collect. Czech. Chem. Commun.
1989, 54, 3260-3266
https://doi.org/10.1135/cccc19893260
The Bayer-Villiger oxidation of diamantanone and the structure of 11-oxo-10-oxapentacyclo[7,4,1,14,13,02,7,06,12]-pentadecane
Jan Ondráčeka, Josef Jankůb, Jiří Novotnýa, Luděk Vodičkab, László Csordásc and Bohumil Kratochvíla
a Department of Solid State Chemistry, Prague Institute of Chemical Technology, 166 28 Prague 6, Czechoslovakia
b Laboratory of Synthetic Fuels, Prague Institute of Chemical Technology, 166 28 Pragur 6, Czechoslovakia
c Laboratory of Surface and Interface Physics, Eotvos University, 1088 Budapest, Hungary
Crossref Cited-by Linking
- Khusnutdinov Ravil I., Egorova Tatyana M., Aminov Rishat I., Dzhemilev Usein M.: Pentafluoroperbenzoic acid as the efficient reagent for Baeyer–Villiger oxidation of cyclic ketones. Mendeleev Communications 2018, 28, 644. <https://doi.org/10.1016/j.mencom.2018.11.027>
- Krasutsky Pavel A., Kolomitsyn Igor V., Kiprof Paul, Carlson Robert M., Fokin Andrey A.: Observation of a Stable Carbocation in a Consecutive Criegee Rearrangement with Trifluoroperacetic Acid. J. Org. Chem. 2000, 65, 3926. <https://doi.org/10.1021/jo991745u>
- Feldman Ken S., Campbell Robert F., West Theodore R., Aloise Allen D., Giampetro David M.: Modeling Chemical Vapor Deposition (CVD) Diamond Film Growth with Diamantane-Derived Radicals in Solution: Permissive Evidence in Support of the Garrison−Brenner Mechanism for Incorporation of Carbon into the Dimer Sites of the {100} Diamond Surface. J. Org. Chem. 1999, 64, 7612. <https://doi.org/10.1021/jo9911793>
