66695-69-0Relevant academic research and scientific papers
An Environmentally Sustainable Mechanochemical Route to Hydroxamic Acid Derivatives
Mocci, Rita,De Luca, Lidia,Delogu, Francesco,Porcheddu, Andrea
supporting information, p. 3135 - 3144 (2016/10/09)
An operationally simple, and cost efficient conversion of carboxylic acids into hydroxamic acid derivatives via a high-energy mechanochemical activation is presented. This ball milling methodology was applied to a wide variety of carboxylic acids dramatically improving purification issues associated with this class of molecules, which still remain one of the main bottlenecks of classical methodologies. (Figure presented.).
Amino acid-based reoxidants for aminohydroxylation: Application to the construction of amino acid-amino alcohol conjugates
Donohoe, Timothy J.,Callens, Cedric K. A.,Flores, Aida,Mesch, Stefanie,Poole, Darren L.,Roslan, Ishmael A.
, p. 10957 - 10960 (2012/01/05)
A viable nitrogen source for the aminohydroxylation reaction of terminal alkenes: By adding a N-O based reoxidant onto an amino acid acyl carbon atom, compounds were obtained that facilitated catalytic turnover and also promoted the conjugation of an amino acid with an alkene. High levels of regioselectivity were observed, as well as good stereoselectivity induced by catalytic amounts of a chiral ligand.
Phthaloyl amino acid hydroxamic acids
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, (2008/06/13)
A series of phthaloyl amino acid hydroxamic acids are useful as inhibitors of Angiotensin I converting enzyme.
