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Showing 1-10 of 10 results for "424749" within Papers
Spectroscopic (FT-IR, FT-Raman, UV and NMR) Investigation on 1-Phenyl-2-Nitropropene by Quantum Computational Calculations.
Xavier S and Periandy S.
Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy (2015)
Nitro alkene derivatives.
Hass HB, et al.
The Journal of Organic Chemistry, 15(1), 8-14 (1950)
A Mori et al.
Chemical & pharmaceutical bulletin, 38(12), 3449-3451 (1990-12-01)
Microbial reduction of 1-phenyl-2-nitro-1-propene (3) was carried out using 57 strains of yeast, 40 strains of aerobic and facultatively anaerobic bacteria and 40 strains of strictly anaerobic bacteria. Nine strains of yeast (Candida tropicalis, etc.,) had the ability to reduce
Gas chromatographic and mass spectral analysis of amphetamine products synthesized from 1-phenyl-2-nitropropene.
DeRuiter J, et al.
Journal of Chromatographic Science, 32(11), 511-519 (1994)
Diego Romano et al.
Microbial cell factories, 13, 60-60 (2014-04-29)
Old Yellow Enzymes (OYEs) are flavin-dependent enoate reductases (EC that catalyze the stereoselective hydrogenation of electron-poor alkenes. Their ability to generate up to two stereocenters by the trans-hydrogenation of the C = C double bond is highly demanded in asymmetric synthesis.
Pawel M Mordaka et al.
Microbiology (Reading, England), 164(2), 122-132 (2017-11-08)
'Ene'-reductases have attracted significant attention for the preparation of chemical intermediates and biologically active products. To date, research has been focussed primarily on Old Yellow Enzyme-like proteins, due to their ease of handling, whereas 2-enoate reductases from clostridia have received
A Sinnema et al.
Bulletin on narcotics, 33(3), 37-54 (1981-01-01)
The paper reviews the most common synthesis of amphetamines which may be found in illicit traffic. Emphasis is laid on the detection, isolation and identification of impurities in illicit amphetamines through gas chromatography and thin-layer chromatography. The latter method was
Organocatalytic diastereo- and enantioselective sulfa-Michael addition to α,β-disubstituted nitroalkenes
Pei QL, et al.
Tetrahedron, 69, 5367-5373 (2013)
Tundo P and Andraos J
Green Syntheses, 119-119 (2014)
Sanjay K Srivastava et al.
Journal of medicinal chemistry, 45(2), 537-540 (2002-01-11)
A new method for the preparation of N-benzylpyrrolomorphinans has been developed. Thus Michael reaction of the benzylimines of oxycodones and oxymorphones with nitrostyrenes gave a series of 4'-aryl-N-benzylpyrrolomorphinans. These were selective delta antagonists of much higher in vitro potency (with
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