90348-16-6Relevant articles and documents
Rhodium-Catalyzed Double Alkyl-Oxygen Bond Cleavage: An Alkyl Transfer Reaction from Bis/Tris(o-alkyloxyphenyl)phosphine to Aryl Acids
Zhou, Hui,Zhang, Jinlong,Yang, Huameng,Xia, Chungu,Jiang, Gaoxi
supporting information, p. 3406 - 3412 (2016/10/21)
An unprecedented rhodium-catalyzed selective cleavage of double alkyl-oxygen bonds of bis/tris(o-alkyloxyphenyl)phosphine has been realized, in which P atom functions as a directing group and simple aryl acids are the methyl group acceptor to provide methyl esters and a quaternary phosphonium salt. The preliminary mechanism was investigated via an 18O labeling experiment and stoichiometric reaction between a Rh-A crystal and an aromatic acid.
Participation of Solvent Dimethylformamide during Attempted Nucleophilic Displacement of Chlorine in Tetrachlorophthalic Anhydride
Ramadas, Sukuru R.,Pillai, Chandrasekaran N.,Bakthavatchalam, Rajagopal
, p. 1059 - 1060 (2007/10/02)
The interaction of tetrachlorophthalic anhydride with dimethylformamide at its reflux temperature either in the presence or absence of an aryl oxide or alkoxide furnishes predominently N,N-dimethyl-2,3,4,5-tetrachlorobenzamide (3) in contrast to the corresponding acid (4), as reported in literature.