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Volumn 44, Issue 23, 2012, Pages 3633-3638
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Samarium diiodide mediated highly diastereoselective conjugate reduction of the α,β-unsaturated ester moiety in heterocyclic compounds
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Author keywords
, unsaturated ester; conjugate; heterocycle; reduction; samarium diiodide
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Indexed keywords
CONJUGATE;
DIASTEREOMERS;
DIASTEREOSELECTIVE;
HETEROCYCLES;
HETEROCYCLIC COMPOUND;
MIXED SOLVENT;
SAMARIUM DIIODIDE;
TETRA-HYDROFURAN;
UNSATURATED ESTERS;
ESTERIFICATION;
ESTERS;
ETHANOL;
ORGANIC SOLVENTS;
REDUCTION;
SAMARIUM;
STEREOSELECTIVITY;
UNSATURATED COMPOUNDS;
SAMARIUM COMPOUNDS;
DIETHYL TRANS 7 METHYL 1 OXO 5 PHENYL 2,3,5,6,9,10 HEXAHYDRO 1H PYRAZOLO[1,2 A][1,2]DIAZOCINE 6,8 DICARBOXYLATE;
ETHYL CIS (2 OXO 3 (4 TOLY)TETRAHYDRO 1H,5H PYRAZOLO[1,2 A]PYRAZOL 1 YL)PROPANOATE;
ETHYL CIS (2 OXO 3 PHENYLTETRAHYDRO 1H,5H PYRAZOLO[1,2 A]PYRAZOL 1 YL)PROPANOATE;
ETHYL CIS 2 (3 BUTYL 7 OXOTETRAHYDRO 1H,5H PYRAZOLO[1,2 A]PYRAZOL 1 YL)PROPANOATE;
ETHYL CIS 2 (3 CYCLOHEXYL 7 OXOTETRAHYDRO 1H,5H PYRAZOLO[1,2 A]PYRAZOL 1 YL)PROPANOATE;
ETHYL CIS 2 [3 (2 FURYL) 7 OXOTETRAHYDRO 1H,5H PYRAZOLO[1,2 A]PYRAZOL 1 YL]PROPANOATE;
ETHYL CIS 2 [3 (2 NAPHTHYL) 7 OXOTETRAHYDRO 1H,5H PYRAZOLO[1,2 A]PYRAZOL 1 YL]PROPANOATE;
ETHYL CIS 2 [3 (3 CHLOROPHENYL) 7 OXOTETRAHYDRO 1H,5H PYRAZOLO[1,2 A]PYRAZOL 1 YL]PROPANOATE;
ETHYL CIS 2 [3 (4 BROMOPHENYL) 7 OXOTETRAHYDRO 1H,5H PYRAZOLO[1,2 A]PYRAZOL 1 YL]PROPANOATE;
ETHYL CIS 2 [3 (4 CHLOROPHENYL) 7 OXOTETRAHYDRO 1H,5H PYRAZOLO[1,2 A]PYRAZOL 1 YL]PROPANOATE;
ETHYL CIS 2 [3 (4 FLUOROPHENYL) 7 OXOTETRAHYDRO 1H,5H PYRAZOLO[1,2 A]PYRAZOL 1 YL]PROPANOATE;
ETHYL CIS 2 [3 (4 ISOPROPYLPHENYL) 7 OXOTETRAHYDRO 1H,5H PYRAZOLO[1,2 A]PYRAZOL 1 YL]PROPANOATE;
ETHYL CIS 2 [3 (4 METHOXYPHENYL) 7 OXOTETRAHYDRO 1H,5H PYRAZOLO[1,2 A]PYRAZOL 1 YL]PROPANOATE;
PYRAZOLONE DERIVATIVE;
SAMARIUM DIIODIDE;
TETRAHYDROPYRAZOLODIACINONE DERIVATIVE;
TETRAHYDROPYRAZOLONE DERIVATIVE;
UNCLASSIFIED DRUG;
ARTICLE;
CHEMICAL ANALYSIS;
CHEMICAL REACTION;
CHEMICAL STRUCTURE;
ROOM TEMPERATURE;
STEREOCHEMISTRY;
SYNTHESIS;
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EID: 84870250321
PISSN: 00397881
EISSN: 1437210X
Source Type: Journal
DOI: 10.1055/s-0032-1317509 Document Type: Article |
Times cited : (3)
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References (94)
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