Results 111 to 120 of about 117,935,502 (148)

Metal-Free Direct Electrochemical Deoxygenation of Benzylic Alcohols. [PDF]

ACS Sustain Chem Eng
Edmonds AG, Walsh DA, Ermanis K, Cuthbertson JD.   +3 more
europepmc   +1 more source

Polystyrene-Poly(acrylic acid) Block Copolymers for Encapsulation of Butyrylcholinesterase into Injectable Nanoreactors. [PDF]

Biomolecules
Fetin PA, Zorin IM, Shaihutdinova ZM, Masson P, Pashirova TN.   +4 more
europepmc   +1 more source

Ammonium Catecholaldehydes as Multifunctional Bioactive Agents: Evaluating Antimicrobial, Antioxidant, and Antiplatelet Activity. [PDF]

Int J Mol Sci
Bogdanov AV, Tagasheva RG, Voloshina A, Lyubina A, Tsivileva O, Kuzovlev AN, Yi W, Samorodov AV, Ziyatdinova GK, Zhiganshina ER, Arsenyev MV, Bukharov SV.   +11 more
europepmc   +1 more source

High Affinity Dimeric Uracil-Based Receptor for the Recognition of Adenine Derivatives through Triplex-like Interactions. [PDF]

J Org Chem
Volpi S, Rivi N, Korom S, Neri M, Knoll W, Corradini R.   +5 more
europepmc   +1 more source

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Arbuzov-type reaction of acylphosphonites and N-alkoxycarbonylimine cations generated in situ with trifluoroacetic anhydride

Tetrahedron Letters, 2012
Abstract A mild procedure for the synthesis of N-protected α-aminoalkylphosphinic acids by the reaction of N,N′ -benzylidene- or N,N′ -alkylidenebiscarbamates, trifluoroacetic anhydride and the corresponding alkylphosphonous acids in methylene chloride or toluene is described.
Maxim Dmitriev, Valery Ragulin
exaly   +2 more sources

Synthesis of Phosphonates via Michaelis-Arbuzov Reaction

Current Organic Synthesis, 2017
Background: Michaelis–Arbuzov reaction has played a key role for the synthesis of dialkyl or diaryl phosphonates by reacting various alkyl or aryl halides with trialkyl or triaryl phosphite.
Naga Raju Chamarthi, Mandava Venkata Basaveswara Rao   +1 more
exaly   +2 more sources

Formation of amino-substituted phosphinyliron complexes [(.eta.5-C5H5)(CO)2Fe{P(O)(NR2)n(OR')2-n}] (n = 1, 2) by the Arbuzov-like dealkylation reaction

Organometallics, 1989
The reaction of (η 5 -C 5 H 5 )(CO) 2 FeCl with stoichiometric amounts of monoamino- and diamino-substituted oxyphosphines, P(NR 2 ) n (OR') 3−n (n=1, 2), generates the isolable cationic oxyphosphine iron complexes as chloride salts, [(η 5 -C 5 H 5 )(CO) 2 Fe{P(NR 2 ) n (OR') 3−n }] + Cl − . The monoaminooxyphosphine iron complexes undergo the Arbuzov-
Hiroshi. Nakazawa, Yasunori. Kadoi, Katsuhiko. Miyoshi   +2 more
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Synthesis of 1,2-Azaphosphacyclanes; Generality of the Mechanism of P=N Alkylation and Arbuzov Reaction

Phosphorus, Sulfur, and Silicon and the Related Elements, 2002
AbstractFor Abstract see ChemInform Abstract in Full Text.
Tatyana A. Mastryukova, Inga M. Aladzheva, Olga V. Bykhovskaya, Dmitrii I. Lobanov, Alexey M. Nemeryuk, Konstantin A. Lyssenko, Pavel V. Petrovskii, Irina L. Odinets   +7 more
openaire   +1 more source

ChemInform Abstract: Arbuzov‐Type Reaction of Acylphosphonites and N‐Alkoxycarbonylimine Cations Generated in situ with Trifluoroacetic Anhydride.

ChemInform, 2012
AbstractThe use of biscarbamates as stable synthetic equivalents of unstable aldehydes renders possible a mild and efficient access to the target compounds, which represent N‐protected phosphinic α,α′‐pseudo dipeptides.
Maxim E. Dmitriev, Valery V. Ragulin
openaire   +1 more source

ChemInform Abstract: REACTIONS WITH AZIRIDINES. XXI. THE MICHAELIS‐ARBUZOV REACTION WITH N‐ACYL AZIRIDINES AND OTHER AMIDOETHYLATIONS AT PHOSPHORUS

Chemischer Informationsdienst, 1980
AbstractDie Phosphorverbindungen (I) reagieren mit N‐Acylaziridinen (II) unter Bildung von β‐Aminoethylphosphonaten (III), wobei eine Gruppenwanderung an den Stickstoff eintritt.
H. STAMM, G. GERSTER
openaire   +1 more source