Synthesis of sterically hindered polychlorinated biphenyl derivatives

Synthesis

Volumn , Issue 7, 2011, Pages 1045-1054

  Joshi, S N ^a   Vyas, S M ^a   Duffel, M W ^a   Parkin, S ^b   Lehmler, H J ^a  

^a UNIVERSITY OF IOWA   (United States)

^b UNIVERSITY OF KENTUCKY   (United States)

Author keywords

biaryls; dihedral angle; palladium; Suzuki cross coupling; Ullmann cross coupling

Indexed keywords

BIARYLS; CATALYST SYSTEM; CONFORMATIONAL FLEXIBILITY; CROSS-COUPLINGS; CRYSTAL STRUCTURE ANALYSIS; SUZUKI COUPLINGS; SUZUKI CROSS-COUPLING; ULLMANN COUPLING REACTION;

CHLORINE; CRYSTAL STRUCTURE; ORGANIC POLLUTANTS; POLYCHLORINATED BIPHENYLS; SYNTHESIS (CHEMICAL);

DIHEDRAL ANGLE;

2,2',3,3',4',6 HEXACHLORO 4 METHOXYBIPHENYL; 2,2',3,3',4',6 HEXACHLORO 4,5 DIMETHOXYBIPHENYL; 2,2',3,3',4',6 HEXACHLORO 5 METHOXYBIPHENYL; 2,2',3,3',4',6 HEXACHLOROBIPHENYL; 2,2',3,3',4',6 HEXACHLOROBIPHENYL 4 OL; 2,2',3,3',4',6 HEXACHLOROBIPHENYL 5 OL; 2,2',3,4',5',6 HEXACHLORO 5 METHOXYBIPHENYL; 2,2',3,4',5',6 HEXACHLOROBIPHENYL 5 OL; 2,2',3,4',6 PENTACHLORO 4 METHOXYBIPHENYL; 2,2',3,4',6 PENTACHLORO 4,5 DIMETHOXYBIPHENYL; 2,2',3,4',6 PENTACHLORO 5 METHOXYBIPHENYL; 2,2',3,4',6 PENTACHLOROBIPHENYL; 2,2',3,4',6 PENTACHLOROBIPHENYL 4 OL; 2,2',3,4',6 PENTACHLOROBIPHENYL 5 OL; 2,2',3,5',6 PENTACHLORO 4 METHOXYBIPHENYL; 2,2',3,5',6 PENTACHLORO 4,5 DIMETHOXYBIPHENYL; 2,2',3,5',6 PENTACHLORO 5 METHOXYBIPHENYL; 2,2',3,5',6 PENTACHLOROBIPHENYL; 2,2',3,5',6 PENTACHLOROBIPHENYL 4 OL; 2,2',3,5',6 PENTACHLOROBIPHENYL 5 OL; 3,5 DICHLORO 2 NITROANISOLE; 3,5 DICHLORO 2 NITROPHENOL; 3,5 DICHLORO 4 NITROANISOLE; 3,5 DICHLORO 4 NITROPHENOL; 3,5 DICHLOROPHENOL; 4 BROMO 2,3,5 TRICHLOROANISOLE; 4 BROMO 3,5 DICHLOROANISOLE; POLYCHLORINATED BIPHENYL DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; BROMINATION; CHEMICAL ANALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; CHLORINATION; COLUMN CHROMATOGRAPHY; CRYSTAL STRUCTURE; CRYSTALLIZATION; HYDROXYLATION; IONIZATION; NITRATION; PROTON NUCLEAR MAGNETIC RESONANCE; SUZUKI REACTION; SYNTHESIS;

EID: 79953029993     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0030-1258454     Document Type: Article

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