2498-46-6Relevant academic research and scientific papers
Two new types of π-conjugation between a fullerene sphere and an addend
Kooistra, Floris B.,Leuning, Tessa M.,Maroto Martinez, Enrique,Hummelen, Jan C.
supporting information; scheme or table, p. 2097 - 2099 (2010/08/22)
Diazirine addition reactions to C60, followed by an HCl elimination step, yielded [6,6] and [5,6] sp2 carbon bridged fullerenes. The [5,6] adducts (alkylidenehomofullerenes) are the first examples of fullerene structures where the ad
Pyrimidine Classical Cannabinoid Compounds and Related Methods of Use
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Page/Page column 6-7, (2009/12/05)
Disclosed are compounds of the formula I: wherein R1, R2, V, W, X, Y and Z can be as defined herein. The compounds can be used in the treatment of disorders mediated by the cannabinoid receptors.
Pyrimidine Non-Classical Cannabinoid Compounds and Related Methods of Use
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Page/Page column 6, (2009/12/05)
Disclosed are compounds of the formula I: wherein R1, R2, V, W, X, Y and Z can be as defined herein. The compounds can be used in the treatment of disorders mediated by the cannabinoid receptors.
Oxime glucokinase activators
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Page/Page column 18, (2008/12/06)
Disclosed herein are pyrazole glucokinase activators of the formula (I): that are useful for the treatment of metabolic diseases and disorders.
REACTIVE INTERMEDIATES IN THE PHOTOLYSIS AND THERMOLYSIS OF 3-CHLORO-3-BENZYLDIAZIRINE
Liu, Michael T. H.,Chishti, Najmul H.,Tencer, Michael,Tomioka, Hideo,Izawa, Yasuji
, p. 887 - 892 (2007/10/02)
The photochemical and thermal decomposition of 3-chloro-3-benzyldiazirine have been studied in different reaction conditions.The decomposition gives rise to benzylchlorocarbene which can rearrange to E and Z chlorostyrene and/or react with the environment.In the presence of acetic acid the main product is 1-chloro-2-phenylethyl acetate.Experiments with acetic acid-d4 showed that some of the chlorostyrene is formed from the carbocation; other experiments conducted with tetramethylethylene as a carbene trapping agent show that the carbene is formed even in the presence of acetic acid.
