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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.
7                Among these interactions, (S)-mandelic acid (10(-3) M) led to over 20-fold fluorescenc
8 reoregular PMA was realized using a pyridine/mandelic acid adduct (PyMA) as an organocatalyst for the
9 ucturally differentiated guests derived from mandelic acid and alpha-amino acids.
10              Chiral carboxylic acids such as mandelic acid and alpha-Br-butyric acid are identified a
11        Pd-catalyzed C-H functionalization of mandelic acid and alpha-phenylglycine is reported.
12 , catalyzes the hydrolysis of mandelamide to mandelic acid and ammonia.
13                             A combination of mandelic acid and N-bromosuccinimide efficiently convert
14    A series of phenylacetic acids, including mandelic acid and phenylglycine, react smoothly with var
15 show that the ethyl and methyl esters of (S)-mandelic acid are substrates for MDH.
16                                              Mandelic acids are prototypic chiral molecules where the
17 antiomer measured in the presence of (+)-(S)-mandelic acid as a chiral solvating agent.
18 or is the best choice for the recognition of mandelic acid because of its greatly increased fluoresce
19                     One novel candidate is a mandelic acid condensation polymer, designated SAMMA.
20 a statistical bias, but the diversity of the mandelic acid crystallization behavior demonstrates that
21 uctures of 21 (F/Cl/Br/CH3/CH3O) substituted mandelic acid derivatives.
22 rugs ibuprofen and flurbiprofen), as well as mandelic acid derivatives.
23                               Simulations of mandelic acid dimers in isolation, water, and toluene do
24 the (S,S)-sensor significantly more than (R)-mandelic acid does.
25     The observed crystallization behavior of mandelic acids does not correspond to any simple "crysta
26                      It is observed that (S)-mandelic acid enhances the fluorescence intensity of the
27                  A benzyl group ortho to the mandelic acid in 1 occupies an area of the protein that
28          In addition, the optically pure (S)-mandelic acid in combination with 2-formylphenylboronic
29           The third approach starting from R-mandelic acid, involving the RCM reaction to install the
30  we find that a combination of rac-BINAP and mandelic acid is critical for achieving anti-Markovnikov
31 esent report that the oxidation of 4-methoxy mandelic acid is mediated by veratryl alcohol.
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
36                                         Poly(mandelic acid) (PMA) is an aryl analogue of poly(lactic
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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