371975-46-1Relevant articles and documents
Catalytic Radical-Polar Crossover Reactions of Allylic Alcohols
Touney, Eric E.,Foy, Nicholas J.,Pronin, Sergey V.
supporting information, p. 16982 - 16987 (2018/12/14)
Radical-polar crossover hydrofunctionalizations of tertiary allylic alcohols are described. Depending on the structure of the catalyst, corresponding epoxides or semipinacol rearrangement products are selectively obtained in good yields. Experimental evidence points to the participation of alkylcobalt complexes as electrophilic intermediates.
N-LINKED LACTAM M1 RECEPTOR POSITIVE ALLOSTERIC MODULATORS
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Page/Page column 57, (2012/12/13)
The present invention is directed to N-linked lactam compounds of general formula (I) which are M1 receptor positive allosteric modulators and that are useful in the treatment of diseases in which the M1 receptor is involved, such as Alzheimer's disease, schizophrenia, pain or sleep disorders. The invention is also directed to pharmaceutical compositions comprising the compounds, and to the use of the compounds and compositions in the treatment of diseases mediated by the M1 receptor.
PYRAZOLO PYRIMIDINE DERIVATIVES
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Paragraph 0332-0333, (2013/03/26)
The present invention relates to pyrazolo pyrimidine derivatives, to methods of preparing these, to combinations and pharmaceutical composition comprising these, and to their use in the treatment of diseases and disorders which may for example involve autoimmune diseases, angiogenesis, pain, and/or inflammatory diseases.
Synthesis of carbo- and heterocyclic aldehydes bearing an adjacent donor group - Ozonolysis versus OsO4/KIO4-oxidation
Mihovilovic, Marko D.,Spina, Markus,Mueller, Bernhard,Stanetty, Peter
, p. 899 - 909 (2007/10/03)
The synthesis of carbo- and heterocyclic aldehydes bearing an ipso-methoxy group is investigated. The synthetic sequence is based on an initial Grignard addition of an olefin to a cyclic ketone followed by methylation of the resulting tertiary alcohol. The terminal olefin serves as precursor for the aldehyde functionality. Oxidation by ozonolysis turned out to depend significantly on the distance of the donor methoxy group. The observed side reactions could be circumvented by applying a one-pot OsO4 mediated diol formation followed by Malaprade oxidation using KIO4. A series of carbo- and heterocyclic precursors were successfully converted to the title products. Springer-Verlag 2004.