Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H8O3 |
| Molecular Weight | 164.158 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC(=O)C(=O)C1=CC=CC=C1
InChI
InChIKey=YLHXLHGIAMFFBU-UHFFFAOYSA-N
InChI=1S/C9H8O3/c1-12-9(11)8(10)7-5-3-2-4-6-7/h2-6H,1H3
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| The [2+2]-photocycloaddition of aromatic aldehydes and ketones to 3,4-dihydro-2-pyridones: regioselectivity, diastereoselectivity, and reductive ring opening of the product oxetanes. | 2001 Oct 15 |
|
| Atropoisomeric quinolinium salt promoting the access to both enantiomeric forms of methyl mandelate: a versatile NADH mimic. | 2002 Oct 7 |
|
| Constraining asymmetric organometallic catalysts within mesoporous supports boosts their enantioselectivity. | 2003 Dec 10 |
|
| Stereoselective generation of vicinal stereogenic quaternary centers by photocycloaddition of 5-methoxy oxazoles to alpha-keto esters: synthesis of erythro beta-hydroxy dimethyl aspartates. | 2004 Apr 21 |
|
| Ru-Catalyzed asymmetric hydrogenation of alpha-ketoesters with CeCl3.7H2O as additive. | 2005 Nov 24 |
|
| Synthesis, properties, and oxidizing ability of areno-annulated 1,3-dimethyl-10-phenylcyclohepta[4,5]pyrrolo[2,3-d]pyrimidine- 2,4(1,3H)-dionylium ions. | 2006 Jan 6 |
|
| Amine degradation by 4,5-epoxy-2-decenal in model systems. | 2006 Mar 22 |
|
| Unusual temperature dependence of enantioselectivity in asymmetric reductions by chiral NADH models. | 2006 May 11 |
|
| N-methyl-(R)-3-(tert-butyl)-sulfinyl-1,4-dihydropyridine: a novel NADH model compound. | 2007 Mar 12 |
|
| Exploiting nanospace for asymmetric catalysis: confinement of immobilized, single-site chiral catalysts enhances enantioselectivity. | 2008 Jun |
|
| [Overview of 40 years' chemical study]. | 2009 Jan |
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| Mechanistic insights on the magnesium(II) ion-activated reduction of methyl benzoylformate with chelated NADH peptide beta-lactam models. | 2009 Sep 4 |
|
| Integration of newly isolated biocatalyst and resin-based in situ product removal technique for the asymmetric synthesis of (R)-methyl mandelate. | 2010 Sep |
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DTXSID9065867
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84256
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239-263-3
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15206-55-0
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23F2045STG
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84835
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SUBSTANCE RECORD
