ライフサイエンスコーパス: mandelic acid

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 s monitoring the enzymatic racemization of R-mandelic acid.

7 eloped via the iodide catalyzed reduction of mandelic acids.

8 Among these interactions, (S)-mandelic acid (10(-3) M) led to over 20-fold fluorescenc

9 reoregular PMA was realized using a pyridine/mandelic acid adduct (PyMA) as an organocatalyst for the

10 ucturally differentiated guests derived from mandelic acid and alpha-amino acids.

11 Chiral carboxylic acids such as mandelic acid and alpha-Br-butyric acid are identified a

12 Pd-catalyzed C-H functionalization of mandelic acid and alpha-phenylglycine is reported.

13 , catalyzes the hydrolysis of mandelamide to mandelic acid and ammonia.

14 A combination of mandelic acid and N-bromosuccinimide efficiently convert

15 A series of phenylacetic acids, including mandelic acid and phenylglycine, react smoothly with var

16 photoredox-catalyzed meta C-H olefination of mandelic acids and their derivatives is described.

17 show that the ethyl and methyl esters of (S)-mandelic acid are substrates for MDH.

18 Mandelic acids are prototypic chiral molecules where the

19 ) bisphosphonates (BPs) equipped with an (R)-mandelic acid as a chiral auxiliary, with final deprotec

20 antiomer measured in the presence of (+)-(S)-mandelic acid as a chiral solvating agent.

21 or is the best choice for the recognition of mandelic acid because of its greatly increased fluoresce

22 One novel candidate is a mandelic acid condensation polymer, designated SAMMA.

23 a statistical bias, but the diversity of the mandelic acid crystallization behavior demonstrates that

24 uctures of 21 (F/Cl/Br/CH3/CH3O) substituted mandelic acid derivatives.

25 eact with molecular oxygen, giving access to mandelic acid derivatives.

26 rugs ibuprofen and flurbiprofen), as well as mandelic acid derivatives.

27 Simulations of mandelic acid dimers in isolation, water, and toluene do

28 the (S,S)-sensor significantly more than (R)-mandelic acid does.

29 The observed crystallization behavior of mandelic acids does not correspond to any simple "crysta

30 ntiopurity both for etiracetam (ee>98 %) and mandelic acid (ee 95 %) enantiomers.

31 It is observed that (S)-mandelic acid enhances the fluorescence intensity of the

32 A-3 and enantiomerically enriched samples of mandelic acid has been observed, indicating the possible

33 We evaluated pyrrole, mandelic acid, imidazole, and acetamide functional group

34 A benzyl group ortho to the mandelic acid in 1 occupies an area of the protein that

35 In addition, the optically pure (S)-mandelic acid in combination with 2-formylphenylboronic

36 The third approach starting from R-mandelic acid, involving the RCM reaction to install the

37 we find that a combination of rac-BINAP and mandelic acid is critical for achieving anti-Markovnikov

38 esent report that the oxidation of 4-methoxy mandelic acid is mediated by veratryl alcohol.

39 and acyclic amine salts were resolved using mandelic acid (MA) and ditoluoyl tartaric acid (DTTA) wi

40 re found to differentiate the enantiomers of mandelic acid (MA) by (1)H NMR spectroscopy in CDCl(3);

41 e highlight how the two racemic compounds RS-mandelic acid (MAN) and RS-etiracetam (ETI) can be combi

42 ermeation of a range of racemates, including mandelic acid (Man), Fmoc-phenylalanine, 1,1'-bi-2-napht

43 -dimorpholinamide derivatives 7 of their (R)-mandelic acid monoesters, which provided access to the i

44 several aromatic acids (protocatechuic acid, mandelic acid, phthalic acid, benzoic acid, and salicyli

45 Poly(mandelic acid) (PMA) is an aryl analogue of poly(lactic

46 ystals containing nicotinamide (NIC) and (R)-mandelic acid (RMA) in numerous stoichiometric ratios (4

47 oquine samples were derivatized with (S)-(+)-mandelic acid tert-butyldimethylsilyl ether, and a cryst

48 lts of roof-shape amines and both isomers of mandelic acid to establish molecular conformation and co

49 An optimized procedure using catalytic mandelic acid under aqueous conditions at room temperatu

50 ent stereoselectivity in the production of S-mandelic acid under aqueous hydrolytic conditions.

51 ss for the conversion of benzaldehyde to (S)-mandelic acid using a combi-CLEA containing three enzyme

52 s protocol for the ortho olefination of free mandelic acids without any directing groups.