106810-75-7Relevant academic research and scientific papers
Decarboxylative Olefination of Activated Aliphatic Acids Enabled by Dual Organophotoredox/Copper Catalysis
Tlahuext-Aca, Adrian,Candish, Lisa,Garza-Sanchez, R. Aleyda,Glorius, Frank
, p. 1715 - 1719 (2018)
Herein, we demonstrate a dual organophotoredox/copper catalytic strategy toward challenging decarboxylative olefination processes proceeding in high yields and selectivities. This operationally simple method uses photoactive organic molecules and Cu(II)-complexes as catalysts to provide rapid access to a wide variety of olefins from inexpensive synthetic and biomass-derived carboxylic acids under mild light-mediated conditions. Mechanistic investigations suggest that the reaction rate for this process is controlled solely by the incident photon flux.
Synthesis and structure-opioid activity relationships of trans-(±)-3,4-Dichloro-N-methyl-N-[4- or 5-hydroxy-2-(1-pyrrolidiny)cyclohexyl]benzeneacetamides
Cheng, Chen-Yu,Chen, Chin-Yuan,Tao, Pao-Luh
, p. 835 - 842 (1997)
To explore the effects of attaching a hydroxy function to the cyclohexane ring of κ-selective opioid N-[2-(1-pyrrolidinyl)cyclohexyl]benzeneacetamides trans-(±)-3,4-dichloro-N-methyl-N-[4- or 5-hydroxy-2-(1-pyrrolidiny)cyclohexyl]benzeneacetamides (1-4) a
A New Approach to Hydroazulenes via Olefin Metathesis
Junga, Heiko,Blechert, Siegfried
, p. 3731 - 3732 (1993)
Several functionalized diolefins cyclize to hydroazulenes (among others) via olefin metathesis with CH3ReO3.These conversions are regioselective and occur with high diastereoselectivity.
SULFIDE ALKYL COMPOUNDS FOR HBV TREATMENT
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Paragraph 0506, (2016/06/28)
The present invention includes a method of inhibiting, suppressing or preventing HBV infection in an individual in need thereof, comprising administering to the individual a therapeutically effective amount of at least one compound of the invention.
USE OF PYRAZOLOBENZOXAZINES IN METHOD OF TREATING CEREBRAL SENESCENCE AND CEREBRAL HYPOXIN
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, (2008/06/13)
Novel pyrazolobenzoxazines of the formula STR1 wherein R is selected from the group consisting of hydrogen, alkyl of 1 to 5 carbon atoms, cycloalkylalkyl or 4 to 7 carbon atoms, alkenyl and alkynyl of 3 to 5 carbon atoms with the proviso that the multiple
