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Volumn 13, Issue 32, 2015, Pages 8669-8675
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An efficient one pot regioselective synthesis of a 3,3′-spiro-phosphonylpyrazole-oxindole framework via base mediated [1,3]-dipolar cycloaddition reaction of the Bestmann - Ohira reagent with methyleneindolinones
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Author keywords
[No Author keywords available]
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Indexed keywords
CHEMICAL REACTIONS;
CYCLOADDITION;
SCAFFOLDS;
1 ,3-DIPOLARCYCLOADDITION;
DIPOLAR CYCLOADDITION REACTION;
FUNCTIONALIZED;
METHYLENEINDOLINONES;
MILD REACTION CONDITIONS;
PYRAZOLES;
REGIOSELECTIVE SYNTHESIS;
SHORT REACTION TIME;
REGIOSELECTIVITY;
DYES, REAGENTS, INDICATORS, MARKERS AND BUFFERS;
INDOLE DERIVATIVE;
OXINDOLE;
PYRAZOLE DERIVATIVE;
SPIRO COMPOUND;
CHEMICAL STRUCTURE;
CHEMISTRY;
CYCLOADDITION;
STEREOISOMERISM;
SYNTHESIS;
CYCLOADDITION REACTION;
INDICATORS AND REAGENTS;
INDOLES;
MOLECULAR STRUCTURE;
PYRAZOLES;
SPIRO COMPOUNDS;
STEREOISOMERISM;
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EID: 84939185671
PISSN: 14770520
EISSN: None
Source Type: Journal
DOI: 10.1039/c5ob01020a Document Type: Article |
Times cited : (45)
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References (84)
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