Results 71 to 80 of about 763 (172)

Autoxidation of N-hydroxyphenylalkylamines: the inhibitory effect of some anions on copper catalysed autoxidation of N-hydroxyphentermine

, 1977
The inhibitory effect of certain electrolytes and buffers on the copper catalysed autoxidation of N-hydroxyphentermine (2-hydroxylamino-2-methyl-1-phenylpropane) has been investigated.
Sven O Eriksson, Gunilla Lundkvist, Ulf Jonsson, Björn Lindeke   +3 more
core   +1 more source

Effects of Harvest Timing on Phytochemical Composition in Lamiaceae Plants under an Environment-Controlled System. [PDF]

Antioxidants (Basel), 2023
Ryu DH, Cho JY, Yang SH, Kim HY.
europepmc   +1 more source

Nitroalkylation and nitroalkenylation reactions of gamma-lactone enolates. A facile ring switch from polysubstituted gamma-lactones to polysubstituted gamma-lactams

, 2004
Michael addition of lithium enolates of g-butyrolactone 1 and a-methyl-g-butyrolactone 10 to (E)-1-nitropropene 2, (E)-bnitrostyrene 3 and (E)-2-nitro-1-phenylpropene 4 is described.
G. PITACCO, G. PETRILLO, E. RIZZATO, P. NITTI, MORGANTI, STEFANO, C. FORZATO, D. SPINELLI, C. DELL'ERBA, NITTI, PATRIZIA, C. TAVANI, SPINELLI, DOMENICO, FORZATO, Cristina, E. VALENTIN, VALENTIN, ENNIO, RIZZATO, EGON, C. DELLERBA, PITACCO, GIULIANA, S. MORGANTI   +17 more
core   +1 more source

Reductions using Clostridium sporogenes [PDF]

, 2014
Clostridium sporogenes was previously shown to be an extraordinary source for unusual reductases. It can catalyze reduction of wide a range of substrates such as nitroalkenes, enoates and nitro compounds, and can be used to generate chiral products ...
Mordaka, Pawel Mateusz
core  

Hydrogen-bonding interactions in the EGS active-site and proposed reaction mechanism of EGS.

, 2013
(A) Hydrogen-bonding network involving the Lys132 side-chain amino group, the 4-hydroxyl group of EMDF, and the bridging water molecule. Inferred hydrogen-atom positions are shown in blue.
Thomas J. Baiga (34891), Gordon V. Louie (34890), John H. Taylor (34894), Eran Pichersky (34896), Snejina M. Spassova (34895), Joseph P. Noel (34897), Marianne E. Bowman (34892), Takao Koeduka (34893)   +7 more
core   +1 more source

Reductions using Clostridium sporogenes [PDF]

Clostridium sporogenes was previously shown to be an extraordinary source for unusual reductases. It can catalyze reduction of wide a range of substrates such as nitroalkenes, enoates and nitro compounds, and can be used to generate chiral products. In
Mordaka, Pawel Mateusz
core   +2 more sources

Synthesis, Structure, and Optical Properties of 1,4-Dithiafulvene-Based Nonlinear Optic-phores

, 2016
Polyenic nonlinear optic (NLO)-phores with a proaromatic 1,4-dithiafulvene electron donor and the little explored 1,1,3-tricyano-2-phenylpropene acceptor have been synthesized. Their configurational and conformational features, ground state polarization,
Silvia Alías (2479909), Santiago Franco (1456816), Aurora Gragera (2479912), Belén Villacampa (2452399), María Jesús Blesa (2479918), Raquel Andreu (1456828), Javier Garín (2479915), Magali Allain (1527463), Jesús Orduna (2452402), Pilar Romero (2031775)   +9 more
core   +1 more source

The clove (Syzygium aromaticum) genome provides insights into the eugenol biosynthesis pathway. [PDF]

Commun Biol, 2022
Ouadi S, Sierro N, Goepfert S, Bovet L, Glauser G, Vallat A, Peitsch MC, Kessler F, Ivanov NV.   +8 more
europepmc   +1 more source

Antibacterial and Biochemical Activities of Phenylpropenes and Monoterpenes on Phytopathogenic Bacteria [PDF]

Journal of Plant Protection and Pathology, 2019
Gehan Marei, S. Abdelgaleil
openaire   +1 more source

Photochemistry of 1-Phenyl-1-diazopropane and Its Diazirine Isomer: A CASSCF and MS-CASPT2 Study. [PDF]

J Phys Chem A, 2022
Soto J.
europepmc   +1 more source