Results 1 to 10 of about 30,405 (153)
Boron Chemistry for Medical Applications [PDF]
Boron compounds now have many applications in a number of fields, including Medicinal Chemistry. Although the uses of boron compounds in pharmacological science have been recognized several decades ago, surprisingly few are found in pharmaceutical drugs.
Fayaz Ali +2 more
doaj +7 more sources
Boron chemistry in a new light. [PDF]
Activation of stable boron species with visible-light allows the creation of boryl and/or carbon radicals through single electron- or energy transfer.
Duret G +3 more
europepmc +4 more sources
Hybrid Boron-Carbon Chemistry [PDF]
The recently proved one-to-one structural equivalence between a conjugated hydrocarbon CnHm and the corresponding borane BnHm+n is applied here to hybrid systems, where each C=C double bond in the hydrocarbon is consecutively substituted by planar B(H2)B
Josep M. Oliva-Enrich +2 more
doaj +4 more sources
Contemporary Research in Boron Chemistry. [PDF]
Guest editors Shih-Yuan Liu and Douglas W. Stephan introduce the Boron Chemistry themed issue of Chemical Society Reviews.
Liu SY, Stephan DW.
europepmc +3 more sources
Metallomimetic Chemistry of Boron [PDF]
The study of main-group molecules that behave and react similarly to transition-metal (TM) complexes has attracted significant interest in recent decades. Most notably, the attractive idea of replacing the all-too-often rare and costly metals from catalysis has motivated efforts to develop main-group-element-mediated reactions.
Marc-André Legare +1 more
exaly +4 more sources
In this review, the history of boron’s early use in drugs, and the history of the use of boron functional groups in medicinal chemistry applications are discussed. This includes diazaborines, boronic acids, benzoxaboroles, boron clusters, and carboranes.
Katia Messner +2 more
doaj +3 more sources
Boron’s Double Edge—Antibiotics, Toxins, and the Fine Line Between Them [PDF]
Boron is a chemically distinctive bioelement whose electron-deficient structure enables reversible coordination with oxygen-rich functional groups such as diols and hydroxyls.
Valery M. Dembitsky +3 more
doaj +2 more sources
Boron-based fire retardancy for natural polymeric materials [PDF]
The shift from fossil resources to natural polymers as the building blocks of a global bioeconomy is hampered by the intrinsic flammability of these bio-derived materials.
Xuan Wang, Sheldon Q. Shi
doaj +2 more sources
Hexafluoroisopropylboranes and -Borates
Novel hexafluoroisopropylboranes (CF3)(CF2H)CFBH2·L and -borate anions [(CF3)(CF2H)CFBH2X]− with Lewis basic heterocyclic ligands L and the anionic substituents X = F− and CN− were obtained.
Ludwig Zapf, Maik Finze
doaj +1 more source
Decaborane: From Alfred Stock and Rocket Fuel Projects to Nowadays
The review covers more than a century of decaborane chemistry from the first synthesis by Alfred Stock to the present day. The main attention is paid to the reactions of the substitution of hydrogen atoms by various atoms and groups with the formation of
Igor B. Sivaev
doaj +1 more source

