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2.
Chem Rev ; 124(5): 2441-2511, 2024 03 13.
Artículo en Inglés | MEDLINE | ID: mdl-38382032

RESUMEN

Boron-containing compounds (BCC) have emerged as important pharmacophores. To date, five BCC drugs (including boronic acids and boroles) have been approved by the FDA for the treatment of cancer, infections, and atopic dermatitis, while some natural BCC are included in dietary supplements. Boron's Lewis acidity facilitates a mechanism of action via formation of reversible covalent bonds within the active site of target proteins. Boron has also been employed in the development of fluorophores, such as BODIPY for imaging, and in carboranes that are potential neutron capture therapy agents as well as novel agents in diagnostics and therapy. The utility of natural and synthetic BCC has become multifaceted, and the breadth of their applications continues to expand. This review covers the many uses and targets of boron in medicinal chemistry.


Asunto(s)
Boranos , Terapia por Captura de Neutrón de Boro , Neoplasias , Humanos , Boro/química , Química Farmacéutica , Compuestos de Boro/química , Neoplasias/tratamiento farmacológico , Ácidos Borónicos , Terapia por Captura de Neutrón de Boro/métodos
3.
Angew Chem Int Ed Engl ; 59(34): 14358-14362, 2020 Aug 17.
Artículo en Inglés | MEDLINE | ID: mdl-32406101

RESUMEN

We report the first trans phosphinoboration of internal alkynes. With an organophosphine catalyst, alkynoate esters and the phosphinoboronate Ph2 P-Bpin are efficiently converted into the corresponding trans-α-phosphino-ß-boryl acrylate products in moderate to good yield with high regio- and Z-selectivity. This reaction operates under mild conditions and demonstrates good atom economy, requiring only a modest excess of the phosphinoboronate. X-ray crystallography experiments allowed structural assignment of the unprecedented and densely functionalized (Z)-α-phosphino-ß-boryl acrylate products.

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