Results 11 to 20 of about 906 (153)
SYNTHESIS AND BIOLOGICAL ACTIⅥTIES OF TRIALKYLTIN DERIVATIVES CONTAINING AZOTIC HETEROCYCLIC COMPOUNDS [PDF]
Xiaojuan Xie +3 more
+5 more sources
Synthesis of Trialkyltin-type Compounds from Dialkyltin-type Compounps
Humio MORI +3 more
openalex +3 more sources
Catch, Cut, or Block? Versatile 4-N-Derivatized Sialyl Glycosides for Influenza Virus Neuraminidase Detection and Purification. [PDF]
Sialyl glycosides containing 4‐N‐derivatized sialic acids synthesized by a highly efficient one‐pot two‐enzyme (OP2E) chemoenzymatic sialylation strategy have been shown to be versatile probes. They can resist sialidase cleavage, be selective substrates by influenza sialidases, or be nanomolar substrate analog‐based inhibitors and affinity ligands ...
Yuan Y +6 more
europepmc +3 more sources
Astatine-211-Towards In Vivo Stable Astatine-211 Labeled Radiopharmaceuticals and Their (Pre)Clinical Applications. [PDF]
ABSTRACT Targeted radioligand therapy has emerged as a promising treatment option for eradicating advanced cancer forms. α‐Emitters are considered particularly promising as they can obliterate (micro)‐metastases. The α‐emitter astatine‐211 (211At) has experienced increased interest due to its favorable decay properties.
Müller M +5 more
europepmc +2 more sources
Organotin(IV) Alkoxides, Siloxides, and Related Stannoxanes. Characterisation and Thermogravimetric Studies. [PDF]
The pendant‐arm ligand [2‐(CH2O)2CH]C6H4 (L) was successfully employed in the isolation of a limited series of organotin(IV) alkoxides and siloxides. A unique example of stannaboroxane was synthesised following a straight‐forward protocol. The thermogravimetric studies performed on the novel organotin(IV) siloxides reveal their potential application as
Penciu V, Bizo L, Varga RA, Someşan AA.
europepmc +2 more sources
Catalytic ipso‐Nitration of Organosilanes Enabled by Electrophilic N‐Nitrosaccharin Reagent
Deploying N‐nitrosaccharin reagents in combination with Lewis acid activation enables the facile, regio‐ and chemoselective nitration of (het)aryl silanes, allowing the introduction of nitro group under unprecedently mild conditions suitable for the late‐stage nitration of complex and polyfunctionalized molecules.
Ivan Mosiagin +5 more
wiley +2 more sources

