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Volumn 69, Issue 42, 2013, Pages 8878-8884
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The organocatalytic enantioselective [3+2] cycloaddition reaction of α,β-unsaturated aldehydes with azomethine ylides applied to the asymmetric synthesis of densely substituted pyrroloisoquinolines
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Author keywords
Cycloaddition; Dipolar reaction; Heterocycles; Organocatalysis; Pyrroloisoquinolines
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Indexed keywords
2,3 UNSATURATED ALDEHYDE;
ALDEHYDE;
AZOMETHINE YLIDE;
DIETHYL 1 (TERT BUTYLDIMETHYLSILYLOXYMETHYL) 8,9 DIMETHOXY 2 METHYL 1,2,5,6 TETRADYROPYRROLO[2,1 A]ISOQUINOLINE 3,3 (10BH)DICARBOXYLATE;
DIETHYL 1 (TERT BUTYLDIMETHYLSILYLOXYMETHYL)2 METHYL 1,2,5,6 TETRAHYDRO[1,3]DIOXOL[4,5 G]PYRROLO[2,1 A]ISOQUINOLINE 3,3 (10BH)DICARBOXYLATE;
DIETHYL 1 (TESRT BUTYLDIMETHYLSILYLOXYMETHYL) 2 METHYL 1,2,5,6 TETRAHYDROPYRROLO[2,1 A]ISOQUINOLINE 3,3(10BH)DICARBOXYLATE;
PYRROLO[2,1 A]ISOQUINOLINE DERIVATIVE;
UNCLASSIFIED DRUG;
ALKYLATION;
ARTICLE;
ASYMMETRIC SYNTHESIS;
CATALYSIS;
CYCLOADDITION;
DIASTEREOISOMER;
DRUG SYNTHESIS;
ENANTIOSELECTIVITY;
PRIORITY JOURNAL;
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EID: 84883490378
PISSN: 00404020
EISSN: 14645416
Source Type: Journal
DOI: 10.1016/j.tet.2013.08.012 Document Type: Article |
Times cited : (10)
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References (32)
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