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Volumn 9, Issue 19, 2011, Pages 6484-6486
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Highly stereoselective synthesis of tetrasubstituted alkenes via hydroamination of alkynes and C-H acetoxylation
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Author keywords
[No Author keywords available]
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Indexed keywords
ACETOXYLATION;
C-H BOND;
DIACETOXYIODOBENZENE;
FUNCTIONALIZATIONS;
FUNCTIONALIZED;
HYDROAMINATIONS;
POTENTIAL METHODS;
STEREOSELECTIVE SYNTHESIS;
ACETYLENE;
CARBONYL COMPOUNDS;
CARBONYLATION;
STEREOCHEMISTRY;
STEREOSELECTIVITY;
SYNTHESIS (CHEMICAL);
OLEFINS;
ALKENE;
ALKYNE;
IODOBENZENE;
AMINATION;
ARTICLE;
CHEMICAL STRUCTURE;
CHEMISTRY;
OXIDATION REDUCTION REACTION;
STEREOISOMERISM;
SYNTHESIS;
ALKENES;
ALKYNES;
AMINATION;
CHEMISTRY TECHNIQUES, SYNTHETIC;
IODOBENZENES;
MOLECULAR STRUCTURE;
OXIDATION-REDUCTION;
STEREOISOMERISM;
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EID: 80052733662
PISSN: 14770520
EISSN: None
Source Type: Journal
DOI: 10.1039/c1ob05958k Document Type: Article |
Times cited : (16)
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References (31)
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