Tetrabutylammonium fluoride (TBAF)-catalyzed addition of substituted trialkylsilylalkynes to aldehydes, ketones, and trifluoromethyl ketones

Journal of Organic Chemistry

Volumn 76, Issue 11, 2011, Pages 4482-4488

  Chintareddy, Venkat Reddy ^a   Wadhwa, Kuldeep ^a   Verkade, John G ^a  

^a IOWA STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EFFICIENT CATALYSTS; ETHYNYL; GOOD YIELD; PRODUCT YIELDS; PROPARGYLIC ALCOHOLS; REACTION CONDITIONS; ROOM TEMPERATURE; TETRABUTYLAMMONIUM FLUORIDES; TRIFLUOROMETHYL; TRIFLUOROMETHYLKETONE; TRIMETHYL;

ACETYLENE; ALCOHOLS; ALDEHYDES; CARBONYLATION; FUNCTIONAL GROUPS; ORGANIC POLYMERS; ORGANIC SOLVENTS; THIOPHENE;

KETONES;

1 PHENYL 2 TRIMETHYLSILYL ACETYLENE; 1 TRIMETHYLSILYL 1 HEXYNE; 2 PYRIDYL KETONE; 3 THIOPHENECARBOXALDEHYDE; ACETYLENE DERIVATIVE; ALCOHOL DERIVATIVE; ALDEHYDE; ALKYNE DERIVATIVE; CARBONYL DERIVATIVE; FUNCTIONAL GROUP; FURAN 3 CARBOXALDEHYDE; KETONE; KETONE DERIVATIVE; PROPARGYL ALCOHOL; QUATERNARY AMMONIUM DERIVATIVE; SILANE DERIVATIVE; SOLVENT; TETRABUTYLAMMONIUM FLUORIDE; TETRAHYDROFURAN; TRIMETHYL (( 4 (TRIFLUOROMETHYL)PHENYL)ETHYNYL)SILANE; TRIMETHYL(THIOPHEN 3 YLETHYNYL)SILANE; UNCLASSIFIED DRUG;

ALKYNYLATION; ARTICLE; ARYLATION; BIOTRANSFORMATION; CATALYST; CHEMICAL COMPOSITION; CONTROLLED STUDY; CYCLOADDITION; QUANTUM YIELD; ROOM TEMPERATURE; SILYLATION; SUBSTITUTION REACTION; SYNTHESIS;

EID: 79957852287     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo200314g     Document Type: Article

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