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221 results

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Page 1
6-(2-Hydroxybenzoyl)-5-(pyrrol-2-yl)-3H-pyrrolizine.
Dey SP, Dey DK, Mallik AK, Dahlenburg L. Dey SP, et al. Acta Crystallogr C. 2003 Jun;59(Pt 6):o321-2. doi: 10.1107/s0108270103008394. Epub 2003 May 20. Acta Crystallogr C. 2003. PMID: 12794351
The title compound, 2-hydroxyphenyl 5-(pyrrol-2-yl)-3H-pyrrolizin-6-yl ketone, C(18)H(14)N(2)O(2), was isolated from the base-catalyzed 1:2 condensation of 2-hydroxyacetophenone with pyrrole-2-carbaldehyde. The pyrrole N-H and hydroxybenzoyl O-H groups are hydrogen …
The title compound, 2-hydroxyphenyl 5-(pyrrol-2-yl)-3H-pyrrolizin-6-yl ketone, C(18)H(14)N(2)O(2), was isolated from the base-catalyzed 1:2 …
Multifunctional asymmetric catalysis.
Shibasaki M, Kanai M. Shibasaki M, et al. Chem Pharm Bull (Tokyo). 2001 May;49(5):511-24. doi: 10.1248/cpb.49.511. Chem Pharm Bull (Tokyo). 2001. PMID: 11383599 Free article. Review.
In the first part of this review, the first example of a catalytic enatioselective nitro-Mannich reaction as well as a direct catalytic enantioselective aldol reaction of 2-hydroxyacetophenone using bimetallic complexes is discussed. The new complex, composed of ytt …
In the first part of this review, the first example of a catalytic enatioselective nitro-Mannich reaction as well as a direct catalytic enan …
Alpha-hydroxyketones as inhibitors of urease.
Tanaka T, Kawase M, Tani S. Tanaka T, et al. Bioorg Med Chem. 2004 Jan 15;12(2):501-5. doi: 10.1016/j.bmc.2003.10.017. Bioorg Med Chem. 2004. PMID: 14723968
Of 13 alpha-hydroxyketones (1-13) tested, 2,2'-thenoin (10) (IC(50)=0.18 mM), furoin (9) (IC(50)=0.36 mM), 2-hydroxy-1-phenylethanone (5) (IC(50)=0.47 mM) and acetol (1) (IC(50)=2.9 mM) showed potent inhibitory activity against the enzyme, comparable w …
Of 13 alpha-hydroxyketones (1-13) tested, 2,2'-thenoin (10) (IC(50)=0.18 mM), furoin (9) (IC(50)=0.36 mM), 2-hydroxy-1- …
Highly enantioselective reduction of 2-hydroxy-1-phenylethanone to enantiopure (R)-phenyl-1,2-ethanediol using Saccharomyces cerevisiae of remarkable reaction stability.
Hu Q, Xu Y, Nie Y. Hu Q, et al. Bioresour Technol. 2010 Nov;101(22):8502-8. doi: 10.1016/j.biortech.2010.06.044. Epub 2010 Jul 13. Bioresour Technol. 2010. PMID: 20630745
Saccharomyces cerevisiae JUC15 was successfully obtained by target reaction-oriented screening, which reduced 2-hydroxy-1-phenylethanone (HPE) to (R)-phenyl-1,2-ethanediol ((R)-PED) of excellent enantiomeric excess (e.e. >99.9%). ...
Saccharomyces cerevisiae JUC15 was successfully obtained by target reaction-oriented screening, which reduced 2-hydroxy-1
2-Hydroxyacetophenone 4-phenylthiosemicarbazone.
Seena EB, Manoj E, Kurup MR. Seena EB, et al. Acta Crystallogr C. 2006 Aug;62(Pt 8):o486-8. doi: 10.1107/S0108270106014776. Epub 2006 Jul 22. Acta Crystallogr C. 2006. PMID: 16891727 No abstract available.
Facile synthesis of 2-hydroxyacetophenone from racemic styrene oxide catalyzed by engineered enzymes.
Söderlund I, Tjärnhage E, Hamnevik E, Widersten M. Söderlund I, et al. Biotechnol Lett. 2022 Aug;44(8):985-990. doi: 10.1007/s10529-022-03271-w. Epub 2022 Jun 22. Biotechnol Lett. 2022. PMID: 35731351 Free PMC article.
Racemic styrene oxide added to growth medium passively enters the cells and is hydrolyzed into (1R)-phenylethane-1,2-diol, which is subsequently oxidized to the acyloin 2-hydroxyacetophenone. Produced 2-hydroxyacetophenone escapes the cells via passive …
Racemic styrene oxide added to growth medium passively enters the cells and is hydrolyzed into (1R)-phenylethane-1,2-diol, which is subseque …
Efficient production of (S)-1-phenyl-1,2-ethanediol using xylan as co-substrate by a coupled multi-enzyme Escherichia coli system.
Rao J, Zhang R, Xu G, Li L, Xu Y. Rao J, et al. Microb Cell Fact. 2020 Apr 7;19(1):87. doi: 10.1186/s12934-020-01344-x. Microb Cell Fact. 2020. PMID: 32264866 Free PMC article.
(S)-carbonyl reductase II from Candida parapsilosis catalyzes the conversion of 2-hydroxyacetophenone to (S)-1-phenyl-1,2-ethanediol with NADPH as a cofactor. Glucose dehydrogenase with a Ala258Phe mutation is able to catalyze the oxidation of xylose with concomitan …
(S)-carbonyl reductase II from Candida parapsilosis catalyzes the conversion of 2-hydroxyacetophenone to (S)-1-phenyl-1,2-etha …
[Characterization of the affinity-tags-regulated (S)-carbonyl reductase 2 towards 2-hydroxyacetophenone reduction].
Li Y, Zhang R, Xu Y. Li Y, et al. Sheng Wu Gong Cheng Xue Bao. 2021 Dec 25;37(12):4277-4292. doi: 10.13345/j.cjb.210088. Sheng Wu Gong Cheng Xue Bao. 2021. PMID: 34984874 Free article. Chinese.
The (S)-carbonyl reductase 2 (SCR2) from Candida parapsilosis can reduce 2-hydroxyacetophenone, which is a valuable prochiral ketones. Different affinity tags, i.e. his-tag, strep-tag and MBP-tag, were attached to the N terminus of SCR2. These tagged SCR2 enzymes, i …
The (S)-carbonyl reductase 2 (SCR2) from Candida parapsilosis can reduce 2-hydroxyacetophenone, which is a valuable prochiral …
Calcium complexation by corticosteroids.
Hauser MR, Doxsee KM, Hope H. Hauser MR, et al. Inorg Chem. 2009 Nov 16;48(22):10780-8. doi: 10.1021/ic901670r. Inorg Chem. 2009. PMID: 19839577
Cortisone and hydrocortisone form calcium complexes of 2:1 steroid/Ca(2+) stoichiometry in solution, with formation constants of 201 +/- 1.7 and 184 +/- 1.7 M(-2), respectively-roughly half the value seen for a simple aromatic alpha-hydroxy ketone, phenacyl alcohol
Cortisone and hydrocortisone form calcium complexes of 2:1 steroid/Ca(2+) stoichiometry in solution, with formation constants of 201 +/- 1.7 …
221 results