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Volumn 1217, Issue 13, 2010, Pages 2050-2055

Enantioseparation and absolute configuration of the atropisomers of a naturally produced hexahalogenated 1,1′-dimethyl-2,2′-bipyrrole

(7) Rosenfelder, Natalie a Ostrowicz, Patrizia a Fu, Liangfeng b Gribble, Gordon W b Tittlemier, Sheryl A c Frey, Wolfgang d Vetter, Walter a

a UNIVERSITY OF HOHENHEIM (Germany)

b Dartmouth College (United States)

c FOOD RESEARCH DIVISION (Canada)

d UNIVERSITY OF STUTTGART (Germany)

Author keywords

Enantiomer fractions; Enantiomer separation; Halogenated dimethyl bipyrrole; Halogenated natural products; Marine mammals

Indexed keywords

BIPYRROLE; ENANTIOMER FRACTIONS; ENANTIOMER SEPARATION; HALOGENATED NATURAL PRODUCTS; MARINE MAMMALS;

CHIRALITY; CHROMATOGRAPHIC ANALYSIS; ENANTIOMERS; GAS CHROMATOGRAPHY; HALOGENATION; HIGH PRESSURE LIQUID CHROMATOGRAPHY; MAMMALS; MASS SPECTROMETRY; NITROGEN COMPOUNDS; POLARIMETERS; SEPARATION;

HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;

5,5' DICHLORO 1,1' DIMETHYL 3,3',4,4' TETRABROMO 2,2' BIPYRROLE; HALOGENATED 1,1' DIMETHYL 2,2' BIPYRROLE DERIVATIVE; NATURAL PRODUCT; PYRROLE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL ANALYSIS; CHIRALITY; CRYSTALLIZATION; ELUTION; ENANTIOSELECTIVITY; ENANTIOSEPARATION; GAS CHROMATOGRAPHY; HALOGENATION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HIGH TEMPERATURE; MASS SPECTROMETRY; PRIORITY JOURNAL; RACEMIZATION; SEPARATION TECHNIQUE; SYNTHESIS;

CHROMATOGRAPHY, HIGH PRESSURE LIQUID; CRYSTALLIZATION; MOLECULAR STRUCTURE; PYRROLES; STEREOISOMERISM;

MAMMALIA;

EID: 77349113738 PISSN: 00219673 EISSN: None Source Type: Journal
DOI: 10.1016/j.chroma.2010.01.083 Document Type: Article

Times cited : (11)

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