Results 111 to 120 of about 1,349 (139)

A novel Cu(OTf)2 mediated three component high yield synthesis of α -aminophosphonates

ARKIVOC, 2006
Abhimanyu S. Paraskar, Arumugam Sudalai
doaj   +1 more source

An expeditious green route toward 2-aryl-4-phenyl-1-imidazoles [PDF]

core   +1 more source

SnCl₂-catalyzed Kabachnik-Fields synthesis of α-aminophosphonates with potent antioxidant activity. [PDF]

RSC Adv
Hibot A, Hamri S, Hafid A, Khouili M, Pujol MD.   +4 more
europepmc   +1 more source

MOF modified with a Cu-complex as a novel MOF-based heterogeneous catalyst for the one-pot one-step synthesis of α-aminophosphonates directly from alcohols by a tandem oxidation process. [PDF]

RSC Adv
Sobhani S, Paseban A, Jahanshahi R, Sansano JM.   +3 more
europepmc   +1 more source

Straightforward continuous synthesis of α-aminophosphonates under microreactor conditions

ARKIVOC, 2005
Ellen Van Meenen, Kristof Moonen, Davy Acke, Christian V. Stevens   +3 more
doaj   +1 more source

Methods for synthesis of N-heterocyclyl/heteroaryl- α-aminophosphonates and α-(azaheterocyclyl)phosphonates

ARKIVOC, 2016
Reda M. Abdel-Rahman, Tarik E. Ali, Somaia M. Abdel-Kariem   +2 more
doaj   +1 more source

Inhibition of DRP-1 mitochondrial mitophagy and fission by novel α-aminophosphonates bearing pyridine: synthesis, biological evaluations, and computer-aided design. [PDF]

BMC Chem
Hekal HA, Salem MM, El Salam HAA.
europepmc   +1 more source

Pharmacological Activities of Schiff Bases and Their Derivatives with Low and High Molecular Phosphonates. [PDF]

Pharmaceuticals (Basel), 2023
Tsacheva I, Todorova Z, Momekova D, Momekov G, Koseva N.   +4 more
europepmc   +1 more source

One-pot synthesis of pyrazolo[4,3-d]thiazole derivatives containing α-aminophosphonate as potential Mur A inhibitors against MDR pathogens with radiosterilization and molecular modeling simulation. [PDF]

RSC Adv, 2023
Ragab A, Ibrahim SA, Aboul-Magd DS, Baren MH.   +3 more
europepmc   +1 more source

Dipeptide analogues of fluorinated aminophosphonic acid sodium salts as moderate competitive inhibitors of cathepsin C. [PDF]

Beilstein J Org Chem, 2023
Wątroba K, Pawełczak M, Kaźmierczak M.   +2 more
europepmc   +1 more source