Selectivity reversal during thia-Michael additions using tetrabutylammonium hydroxide: Operationally simple and extremely high turnover

Synthesis (Germany)

Volumn 46, Issue 13, 2014, Pages 1725-1730

  Nicponski, Daniel R ^a   Marchi, Jennifer M ^a  

^a PURDUE UNIVERSITY   (United States)

Author keywords

catalysis; conjugate addition; green chemistry; high turnover number; selectivity reversal; thia Michael reaction

Indexed keywords

ADDITION REACTIONS; CATALYSIS; CATALYSTS; CHEMICAL COMPOUNDS;

CATALYTIC LOADING; CONJUGATE ADDITION; GREEN CHEMISTRY; MICHAEL ACCEPTORS; TETRABUTYLAMMONIUM HYDROXIDES; THIA-MICHAEL REACTION; TURNOVER NUMBER;

LOADING;

TETRABUTYLAMMONIUM; TETRABUTYLAMMONIUM HYDROXIDE; THIOL; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CATALYST; CHEMICAL REACTION KINETICS; CONJUGATION; MICHAEL ADDITION; SYNTHESIS; THIA MICHAEL ADDITION; TURNOVER TIME;

EID: 84903313729     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0033-1341106     Document Type: Article

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