Herein we present the synthesis of b-mono and b-bis-substituted vinylidenebisphosphonate esters bearing a carboxylic ester moiety to be used as building blocks for further functionalizations. Reactions of these new bisphosphonate scaffolds through hydrogenation of the unsaturated CQC bond and through metal mediated addition of aryl boronic acids and indoles provide a wide range of new bisphosphonate products as potential leads to contrast osteoporosis.

Functional bisphosphonate synthesis for the development of new anti-resorption bone drug candidates

Enrica Bortolamiol
Membro del Collaboration Group
;
Andrea Chiminazzo
Membro del Collaboration Group
;
Laura Sperni
Membro del Collaboration Group
;
Giuseppe Borsato
Membro del Collaboration Group
;
Fabrizio Fabris
Project Administration
;
Alessandro Scarso
Project Administration
2019-01-01

Abstract

Herein we present the synthesis of b-mono and b-bis-substituted vinylidenebisphosphonate esters bearing a carboxylic ester moiety to be used as building blocks for further functionalizations. Reactions of these new bisphosphonate scaffolds through hydrogenation of the unsaturated CQC bond and through metal mediated addition of aryl boronic acids and indoles provide a wide range of new bisphosphonate products as potential leads to contrast osteoporosis.
2019
43
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10278/3719247
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