Carbaboranes as pharmacophores: properties, synthesis, and application strategies
M Scholz, E Hey-Hawkins - Chemical Reviews, 2011 - ACS Publications
Medicinal chemistry is still clearly dominated by organic chemistry. Most of the marketed
drugs are purely organic molecules. The right-hand neighbors of carbon in the periodic …
drugs are purely organic molecules. The right-hand neighbors of carbon in the periodic …
Boron science
NS Hosmane - New technologies and applications, 2011 - api.taylorfrancis.com
What is boron? The question itself may not seem very significant to many people. Their
introduction to the word “boron” could come as the butt of a joke. Conan O'Brien made jokes …
introduction to the word “boron” could come as the butt of a joke. Conan O'Brien made jokes …
[HTML][HTML] Recent advances in transition metal-mediated functionalization of o-carboranes
Z Qiu - Tetrahedron Letters, 2015 - Elsevier
Icosahedral carboranes constitute a class of structurally unique molecules with exceptionally
thermal and chemical stabilities, which limits the derivatization of these clusters. In view of …
thermal and chemical stabilities, which limits the derivatization of these clusters. In view of …
Direct cupration of fluoroform
A Zanardi, MA Novikov, E Martin… - Journal of the …, 2011 - ACS Publications
We have found the first reaction of direct cupration of fluoroform, the most attractive CF3
source for the introduction of the trifluoromethyl group into organic molecules. Treatment of …
source for the introduction of the trifluoromethyl group into organic molecules. Treatment of …
Blue Phosphorescent Zwitterionic Iridium(III) Complexes Featuring Weakly Coordinating nido-Carborane-Based Ligands
JC Axtell, KO Kirlikovali, PI Djurovich… - Journal of the …, 2016 - ACS Publications
We report the development of a new class of phosphorescent zwitterionic bis (heteroleptic) Ir
(III) compounds containing pyridyl ligands with weakly coordinating nido-carboranyl …
(III) compounds containing pyridyl ligands with weakly coordinating nido-carboranyl …
Metal-catalyzed B–H acylmethylation of pyridylcarboranes: access to carborane-fused indoliziniums and quinoliziniums
HJ Cao, X Wei, F Sun, X Zhang, C Lu, H Yan - Chemical Science, 2021 - pubs.rsc.org
Metal-catalyzed mono-acylmethylation of pyridylcarboranes has been realized using α-
carbonyl sulfoxonium ylides as a coupling partner. The reaction features high efficiency …
carbonyl sulfoxonium ylides as a coupling partner. The reaction features high efficiency …
Potent estrogen agonists based on carborane as a hydrophobic skeletal structure: a new medicinal application of boron clusters
Y Endo, T Iijima, Y Yamakoshi, H Fukasawa… - Chemistry & Biology, 2001 - cell.com
Abstract Background: Carboranes (dicarba-closo-dodecaboranes) are a class of carbon-
containing polyhedral boron-cluster compounds having remarkable thermal stability and …
containing polyhedral boron-cluster compounds having remarkable thermal stability and …
Potent Estrogenic Agonists Bearing Dicarba-closo-dodecaborane as a Hydrophobic Pharmacophore
Y Endo, T Iijima, Y Yamakoshi… - Journal of medicinal …, 1999 - ACS Publications
Introduction. The carboranes (dicarba-closo-dodecaboranes) 1 exhibit remarkable thermal
stability, are resistant to attack by most types of reagents, and are generally biologically …
stability, are resistant to attack by most types of reagents, and are generally biologically …
Enhanced π-conjugation and emission via icosahedral carboranes: Synthetic and spectroscopic investigation
BP Dash, R Satapathy, ER Gaillard, KM Norton… - Inorganic …, 2011 - ACS Publications
The ability of ortho-, meta-and para-carboranes to enhance the emission intensity has been
compared. For this purpose a series of carborane-appended 1, 3, 5-triphenylbenzene (TB) …
compared. For this purpose a series of carborane-appended 1, 3, 5-triphenylbenzene (TB) …
Structure–Activity Relationship of para-Carborane Selective Estrogen Receptor β Agonists
D Sedlák, TA Wilson, W Tjarks… - Journal of Medicinal …, 2021 - ACS Publications
Selective agonism of the estrogen receptor (ER) subtypes, ERα and ERβ, has historically
been difficult to achieve due to the high degree of ligand-binding domain structural similarity …
been difficult to achieve due to the high degree of ligand-binding domain structural similarity …