Results 61 to 70 of about 14,652 (153)

Cobaltabis(Dicarbollide) [o-COSAN]⁻ for Boron Neutron Capture Therapy of Head and Neck Cancer: Biodistribution and Irradiation Studies in an Experimental Oral Cancer Model

Pharmaceuticals
Background: Boron neutron capture therapy (BNCT) is a tumor-selective particle radiotherapy that combines preferential boron accumulation in tumors and neutron irradiation.
Mónica A. Palmieri, Andrea Monti Hughes, Verónica A. Trivillin, Marcela A. Garabalino, Paula S. Ramos, Silvia I. Thorp, Paula Curotto, Emiliano C. C. Pozzi, Miquel Nuez Martínez, Francesc Teixidor, Clara Viñas, Amanda E. Schwint   +11 more
doaj   +1 more source

Palladium-Catalyzed Heck Reactions of Styrene Derivatives and 2-Iodo-p-carborane

, 2016
p-Carborane has been vinylated on the 2-B-atom in high yields using the Heck reaction. Thus, the reaction between 2-iodo-p-carborane and various styrenes [4-H-, 4-C6H4-, 4-Cl-, 4-Br-, 4-NO2-, 4-CH3O-, and 4-CH3-] resulted in the production of the ...
Rodrigo Tascon Claro (3033471), Stefan Sjöberg (2978637), Ludvig Eriksson (3033477), Karl Johan Winberg (3033474)   +3 more
core   +1 more source

Stable exo-nido-Metallacarboranes (M = Os^IV) that Incorporate meta-Carborane-Based Dicarbollide Ligands

, 2016
Reactions of the [K]+ salts of the [nido-7,9-C2B9H12]- anion (2) and its C-phenylated derivative [7-Ph-nido-7,9-C2B9H11]- (4) with [OsCl2(PPh3)3] (3) proceed in benzene at ambient temperature with the formation of 16-electron chlorohydrido-Os(IV) exo ...
Alexander I. Yanovsky (2499058), Galina D. Kolomnikova (2499055), Oleg L. Tok (2499052), Elena V. Balagurova (2499049), Fedor M. Dolgushin (1612729), Dmitri N. Cheredilin (2499046), Igor T. Chizhevsky (2046805)   +6 more
core   +3 more sources

THE INTERMEDIATE DICARBA-NIDO-BORANES

, 2020
The formation of several nido-carboranes, their structures, chemistry, some comparisons with nido-boranes and general stability rules are briefly reviewed.
S Hekmanek, J Pleek
core  

Carborane-Containing Liquid Crystals:  Synthesis and Structural, Conformational, Thermal, and Spectroscopic Characterization of Diheptyl and Diheptynyl Derivatives of p-Carboranes^†

, 2016
Molecular and electronic structures for four p-carborane derivatives were studied in the context of their liquid crystalline properties. Thus molecular and crystal structures of diheptyl and diheptynyl derivatives of 10- and 12-vertex bi-p-carboranes ...
Victor G. Young (1405513), Piotr Kaszynski (1841020), Serhii Pakhomov (2390707), Kris F. Tesh (2964687)   +3 more
core   +2 more sources

Correction to "closo- or nido-Carborane Diphosphane as Responsible for Strong Thermochromism or Time Activated Delayed Fluorescence (TADF) in [Cu(N^N)(P^P)]^0/+". [PDF]

Inorg Chem, 2022
Alconchel A, Crespo O, García-Orduña P, Gimeno MC.   +3 more
europepmc   +1 more source

Synthesis and radioiodination of a nido-1,2-carboranyl derivative of 2-nitroimidazole

, 1994
The synthesis of a nido-carboranyl congener of misonidazole, 1-(3′-nido-carboranyl-2′-hydroxy)propyl-2-nitroimidazole, has been carried out. Alternative methods of preparations were conducted to optimize the chemical yield, with a five step synthesis ...
Livesey, John C., Laramore, George E., Srivastava, Rajiv R., Hamlin, Donald K., Wilbur, D. Scott, Griffin, Thomas W.   +5 more
core   +1 more source

Closo- or Nido-Carborane Diphosphane as Responsible for Strong Thermochromism or Time Activated Delayed Fluorescence (TADF) in [Cu(N^N)(P^P)]^0/. [PDF]

Inorg Chem, 2021
Alconchel A, Crespo O, García-Orduña P, Gimeno MC.   +3 more
europepmc   +1 more source

Synthesis and Structure of Nido-Carboranyl Azide and Its “Click” Reactions

, 2021
Novel zwitter-ionic nido-carboranyl azide 9-N3(CH2)3Me2N-nido-7,8-C2B9H11 was prepared by the reaction of 9-Cl(CH2)3Me2N-nido-7,8-C2B9H11 with NaN3.
Druzina Anna A
core  

THE SYNTHESIS AND EVALUATION OF CARBORANE SERMS

, 2010
A stereoselective synthesis of closo carborane analogues of Tamoxifen was developed where the products represent a new platform for developing metabolically robust Selective Estrogen Receptor Modulators (SERMs).
Beer, Michael L.
core   +1 more source