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Volumn 45, Issue 23, 2013, Pages 3251-3254
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An improved synthesis of a hydroxymethyl tricyclic ketone from cyclohexanone, the key processes for the synthesis of a highly potent anti-inflammatory and cytoprotective agent
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Author keywords
anti inflammatory agents; antitumor agents; oxidation; reduction; reductive methylation; regioselectivity
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Indexed keywords
ANTI-INFLAMMATORIES;
ANTI-INFLAMMATORY AGENTS;
ANTI-TUMOR AGENTS;
CYCLOHEXANONES;
KEY PROCESS;
ALKYLATION;
CHEMICAL COMPOUNDS;
DRUG PRODUCTS;
KETONES;
OXIDATION;
REDUCTION;
REGIOSELECTIVITY;
METHANOL;
10A ETHINYL 4B,8,8 TRIMETHYL 3,7 DIOXO 3,4B,7,8,8A,9,10,10A OCTAHYDROPHENANTHRENE 2,6 DICARBONITRILE;
8A (HYDROXYMETHYL) 1,1,4A TRIMETHYL 3,4,4A,6,7,8,8A,9,10,10A DECAHYDROPHENANTHREN 2(1H)ONE;
ANTIINFLAMMATORY AGENT;
CYCLOHEXANONE;
HYDROXYMETHYL TRICYCLIC KETONE;
KETONE DERIVATIVE;
PROTECTIVE AGENT;
TBE 31;
UNCLASSIFIED DRUG;
ARTICLE;
CELL PROTECTION;
CHEMICAL REACTION;
DRUG POTENCY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;
PHYSICAL CHEMISTRY;
REACTION ANALYSIS;
STEREOCHEMISTRY;
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EID: 84888134099
PISSN: 00397881
EISSN: 1437210X
Source Type: Journal
DOI: 10.1055/s-0033-1339900 Document Type: Article |
Times cited : (15)
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References (8)
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