Results 81 to 90 of about 715 (176)

Ni/Photoredox-Catalyzed C(sp³)-C(sp³) Coupling between Aziridines and Acetals as Alcohol-Derived Alkyl Radical Precursors. [PDF]

J Am Chem Soc, 2022
Dongbang S, Doyle AG.
europepmc   +1 more source

Ethylamines ((C2H5) n NH3-n)

, 1986
Norio HAKUTA
core   +1 more source

Enantio- and regioselective nickel/photoredox-catalyzed cross-electrophile coupling of benzylic aziridines with alkynyl bromides. [PDF]

Sci Adv
Lan H, Xu ZD, Shi Z, Ackermann L, Wang D.   +4 more
europepmc   +1 more source

Covalent Modification of the JH2 Domain of Janus Kinase 2. [PDF]

ACS Med Chem Lett, 2022
Henry SP, Liosi ME, Ippolito JA, Menges F, Newton AS, Schlessinger J, Jorgensen WL.   +6 more
europepmc   +1 more source

From 2-(2-Acylaryl)ethylamines

, 2005
M. lvarez, J. A. Joule
core   +1 more source

Deprotection of N1-methyladenosine-containing RNA using triethylamine hydrogen fluoride. [PDF]

Nucleosides Nucleotides Nucleic Acids
Apostle A, Fang S.
europepmc   +1 more source

Visible-light-mediated catalyst-free synthesis of unnatural α-amino acids and peptide macrocycles. [PDF]

Nat Commun, 2021
Wang M, Wang C, Huo Y, Dang X, Xue H, Liu L, Chai H, Xie X, Li Z, Lu D, Xu Z.   +10 more
europepmc   +1 more source

Characterisation of Antisense Oligonucleotides by Ion-Pair Reversed-Phase UHPLC-HRMS: Method development using Design of Experiments. [PDF]

J Mass Spectrom
Triolo A, Tavani F, Barnini P, Furlanetto S, Orlandini S.   +4 more
europepmc   +1 more source

Triethylamine-Promoted Oxidative Cyclodimerization of 2H-Azirine-2-carboxylates to Pyrimidine-4,6-dicarboxylates: Experimental and DFT Study. [PDF]

Molecules, 2023
Zakharov TN, Sakharov PA, Novikov MS, Khlebnikov AF, Rostovskii NV.   +4 more
europepmc   +1 more source

The Synthesis of 14C Labelled Serotonin/2-(5' -Hydroxyindolyl-3')-ethylamine-[l-14C]/

, 1957
By modification of published procedure s on the 2-(indolyl)-3') ethylamines syntheses it' was possible to obtain 2-(5'-benzylox yindolyl-3')-acetonitrile-[1-14C) (III) in a 820/o yield, from equimolar amounts of 5-benzyloxygramine methosulphate (II) (1.1
Keglević-Brovet, D., Iskrić, S., S. Iskrić, S. Kveder, D. Keglević-Brovet, Kveder, S.   +5 more
core