51285-23-5Relevant academic research and scientific papers
The use of borane-amine adducts as versatile palladium-catalyzed hydrogen-transfer reagents in methanol
Couturier, Michel,Andresen, Brian M.,Tucker, John L.,Dubé, Pascal,Brenek, Steven J.,Negri, Joanna T.
, p. 2763 - 2766 (2001)
The scope of borane-amine adducts as reducing agents is broadened through palladium-catalyzed methanolysis capable of reducing a wide variety of functional groups. Hence, borane mediated reduction of a benzamide followed by a tandem methanolysis/hydrogenolysis of the resulting borane-benzylamine adduct allows chemoselective removal of an N-benzoyl in the presence of an O-benzoyl.
ACYLATION REACTION OF HYDROXYL GROUP
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Page/Page column 11, (2010/07/03)
Disclosed is a selective ester production process of an alcoholic hydroxyl group, which proceeds under chemically mild conditions, while having adequate environmental suitability, operability and economical efficiency. Specifically disclosed is a process for producing an ester compound, which is characterized in that an alcohol and a carboxylic acid ester compound are reacted in the presence of a compound containing zinc element, thereby selectively acylating a hydroxyl group of the alcohol.
Process for pyrrolidinyl hydroxamic acid compounds
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, (2008/06/13)
A method for preparing hydroxamic acid derivatives which are useful as analgesic, antiinflammatory, or neuroprotective agents.
Syntheses of new modified Phe-Pro peptides. Use of proline replacements in potential HIV inhibitors
Bouygues,Medou,Quelever,Chermann,Camplo,Kraus
, p. 277 - 280 (2007/10/03)
The syntheses consisting of replacement of proline amino acid by a 3-pyrrolidinone ring in Phe-Pro analogues are described. Preliminary anti-HIV studies demonstrated the potential activity of this new class of compounds.
