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Org Lett ; 17(22): 5544-6, 2015 Nov 20.
Article in English | MEDLINE | ID: mdl-26509219

ABSTRACT

The convergent total synthesis of the marine natural product phosphoiodyn A, a nanomolar agonist of human peroxisome proliferator-activated receptor delta (hPPARδ), was achieved in five steps total from commercially available and inexpensive starting materials. The synthesis relies on the unprecedented regioselective hydrozirconation of a terminal acetylene in the presence of a conjugated 1,3-diyne and on ammonolysis of a ß-chlorophosphonic acid monoester. The scheme also provides the newly isolated placotylene A, an inhibitor of bone marrow-derived macrophage (BMM) differentiation.


Subject(s)
Diynes/chemical synthesis , Fatty Alcohols/chemical synthesis , Hydrocarbons, Iodinated/chemical synthesis , Organophosphorus Compounds/chemical synthesis , Polyynes/chemical synthesis , Acetylene/chemistry , Cell Differentiation , Diynes/chemistry , Diynes/pharmacology , Fatty Alcohols/chemistry , Fatty Alcohols/pharmacology , Humans , Hydrocarbons, Iodinated/chemistry , Hydrocarbons, Iodinated/pharmacology , Macrophages/drug effects , Molecular Structure , Organophosphorus Compounds/chemistry , Organophosphorus Compounds/pharmacology , PPAR delta/agonists , Polyynes/chemistry , Polyynes/pharmacology
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