Multigram synthesis of a chiral substituted indoline via copper-catalyzed alkene aminooxygenation

Synthesis

Volumn 44, Issue 10, 2012, Pages 1481-1484

  Sequeira, Fatimac ^a   Bovino, Michaelt ^a   Chipre, Anthonyj ^a   Chemler, Sherryr ^a  

^a UNIVERSITY AT BUFFALO   (United States)

Author keywords

alkene; aminooxygenation; copper catalyzed; indoline; TEMPO

Indexed keywords

AMINOOXYGENATION; COPPER-CATALYZED; ENANTIOSELECTIVE; GRAM-SCALE SYNTHESIS; INDOLINE; MULTIGRAM SYNTHESIS; REDUCED PRESSURE; TEMPO;

CATALYSIS; DISTILLATION; OLEFINS;

COPPER;

2,2 BIS[2 (4,5 DIPHENYL 1,3 OXAZOLINYL)]PROPANE; 5 FLUORO 2 (2,2,6,6 TETRAMETHYLPIPERIDIN 1 YLOXYMETHYL) 1 TOSYLINDOLINE; ALKENE DERIVATIVE; ANILINE DERIVATIVE; COPPER; INDOLE DERIVATIVE; INDOLINE; N (2 ALLYL 4 FLUOROPHENYL) 4 METHYLBENZENESULFONAMIDE; N ALLYL 4 FLUOROANILINE; N,N DIALLYLANILINE; UNCLASSIFIED DRUG;

AMINOOXYGENATION; ARTICLE; CATALYSIS; CATALYST; CHEMICAL PARAMETERS; CHEMICAL REACTION KINETICS; CHEMICAL STRUCTURE; CHIRALITY; CRYSTALLIZATION; DISTILLATION; ENANTIOSELECTIVITY; LIGAND BINDING; MULTIGRAM SCALE; OXYGENATION; STRUCTURE ANALYSIS; SUBSTITUTION REACTION; SYNTHESIS;

EID: 84860289945     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0031-1289762     Document Type: Article

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