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1 eniently resolved via their acetals with (R)-mandelic acid.
2 enantioselective fluorescent recognition of mandelic acid.
3 er and this is demonstrated using lactic and mandelic acid.
4 interaction of (S,S)- and (R,R)-sensors with mandelic acid.
5 y related to the enantiomeric composition of mandelic acid.
6 eloped via the iodide catalyzed reduction of mandelic acids.
8 reoregular PMA was realized using a pyridine/mandelic acid adduct (PyMA) as an organocatalyst for the
14 A series of phenylacetic acids, including mandelic acid and phenylglycine, react smoothly with var
18 or is the best choice for the recognition of mandelic acid because of its greatly increased fluoresce
20 a statistical bias, but the diversity of the mandelic acid crystallization behavior demonstrates that
25 The observed crystallization behavior of mandelic acids does not correspond to any simple "crysta
30 we find that a combination of rac-BINAP and mandelic acid is critical for achieving anti-Markovnikov
32 re found to differentiate the enantiomers of mandelic acid (MA) by (1)H NMR spectroscopy in CDCl(3);
33 ermeation of a range of racemates, including mandelic acid (Man), Fmoc-phenylalanine, 1,1'-bi-2-napht
34 -dimorpholinamide derivatives 7 of their (R)-mandelic acid monoesters, which provided access to the i
35 several aromatic acids (protocatechuic acid, mandelic acid, phthalic acid, benzoic acid, and salicyli
37 ystals containing nicotinamide (NIC) and (R)-mandelic acid (RMA) in numerous stoichiometric ratios (4
38 oquine samples were derivatized with (S)-(+)-mandelic acid tert-butyldimethylsilyl ether, and a cryst
39 lts of roof-shape amines and both isomers of mandelic acid to establish molecular conformation and co
40 ss for the conversion of benzaldehyde to (S)-mandelic acid using a combi-CLEA containing three enzyme
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