Production of mixed halogenated congeners of the natural product heptachloro-1′-methyl-1,2′-bipyrrole (Q1) by photolysis in the presence of bromine

Journal of Chromatography A

Volumn 1216, Issue 36, 2009, Pages 6433-6440

  Gaul, Simon ^a   Vetter, Walter ^a  

^a UNIVERSITY OF HOHENHEIM   (Germany)

Author keywords

Bromination; GC ECNI MS; Halogenated natural products; Mixed halogenated compounds; Photolysis; Structure determination

Indexed keywords

BROMINATION; GC/ECNI-MS; HALOGENATED NATURAL PRODUCTS; MIXED HALOGENATED COMPOUNDS; STRUCTURE DETERMINATION;

BROMINE; CHLORINE; HALOGEN COMPOUNDS; IRRADIATION; ISOMERS; ORGANIC COMPOUNDS; PHOTOLYSIS; WATER WELL PUMPS;

HALOGENATION;

BROMINE; CHLORINE; HEPTACHLORO 1' METHYL 1,2' BIPYRROLE DERIVATIVE; NATURAL PRODUCT; ORGANOHALOGEN DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; BROMINATION; CHEMICAL STRUCTURE; ELUTION; HALOGENATION; ISOMER; PHOTOLYSIS; PRIORITY JOURNAL; ROOM TEMPERATURE; STRUCTURE ANALYSIS; ULTRAVIOLET IRRADIATION;

ADIPOSE TISSUE; ANIMALS; ANISOLES; AUSTRALIA; BIOLOGICAL PRODUCTS; BROMINE; DOLPHINS; GAS CHROMATOGRAPHY-MASS SPECTROMETRY; HALOGENATION; HYDROCARBONS, CHLORINATED; HYDROCARBONS, HALOGENATED; ION EXCHANGE; MOLECULAR STRUCTURE; PHOTOLYSIS; PYRROLES; ULTRAVIOLET RAYS;

CETACEA;

EID: 68549090862     PISSN: 00219673     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.chroma.2009.07.033     Document Type: Article

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