33979-03-2Relevant articles and documents
A Suzuki-type cross-coupling reaction of arylacetylene halides with arylboronic acids
Shi, Yu,Li, Xiaoyu,Liu, Jianhui,Jiang, Wenfeng,Sun, Licheng
experimental part, p. 514 - 520 (2012/04/04)
A PdCl2-catalyzed direct alkynylation of arylboronic acids to give diarylacetylenes is described. The optimal conditions using PdCl 2 as catalyst, MeOH-PhMe-H2O as solvent and K 2CO3 as base effectively suppressed the formation of homo-coupling product and afforded moderate to good yield of the desired unsymmetrical coupling product. This reaction represents a Suzuki-type sp 2(C-B)-sp(C-X) cross-coupling. Copyright
Physical, spectral and chromatographic properties of all 209 individual PCB congeners
Bolgar,et al.
, p. 2687 - 2705 (2007/10/03)
Through the use of two capillary GC columns: 40% octadecyl/ 15% phenyl methyl siloxane and 50% phenyl methyl siloxane, it was possible to separate 201 PCB congeners with only four unresolved pairs. The data compiled in this study for all 209 congeners will aid in the identification of selected individual components of these environmental pollutants. The use of this data also presents the opportunity for the improved quantification of the commercial PCB formulations. -from Authors
New Azoolefines and their Acidic Cleavage to Aryldiimines
Kirschke, Klaus,Moeller, Angela,Schmitz, Ernst
, p. 893 - 898 (2007/10/02)
3-Amino-1-aryl-3',3'-dimethyl-pyrazolin-4-spiro-2'-oxiran-5-ones (3a-c) undergo ring opening with methoxide forming methyl 3-amino-3-arylazo-propenoates (5a-c). 5a-c are cleaved under acidic conditions.The main products of the cleavage of 5c with methanolic hydrochloric acid are nitrogen, 2,4,6-trichloro-benzene (6), 2,4,6-trichloro-aniline (9) and 2,4,6-trichloro-phenylhydrazine (10).Intermediates of the cleavage of 5 are aryldiimines trapped with benzaldehyde as the corresponding benzhydrazides (12a,b).