7072-01-7Relevant articles and documents
Aryllithiums with increasing steric crowding and lipophilicity prepared from chlorides in diethyl ether. the first directly prepared room-temperature-stable dilithioarenes
Screttas, Constantinos G.,Steele, Barry R.,Micha-Screttas, Maria,Heropoulos, Georgios A.
supporting information, p. 5680 - 5683 (2013/01/15)
A convenient procedure has been developed for the preparation of synthetically useful, room-temperature-stable aryllithiums starting from aryl chlorides and lithium metal. The method provides a route to aryllithiums which have previously not been accessible cleanly or could only be prepared by using more expensive starting materials.
Self-assembly and traveling wave ion mobility mass spectrometry analysis of hexacadmium macrocycles
Chan, Yi-Tsu,Li, Xiaopeng,Soler, Monica,Wang, Jin-Liang,Wesdemiotis, Chrys,Newkome, George R.
supporting information; experimental part, p. 16395 - 16397 (2010/02/15)
(Graph Presented) Self-assembly of 1,3-di(4′-terpyridinyl)arenes by using the labile tpy-Cd(II)-tpy (where tpy = 2,2′:6′,2″- terpyridine) connectivity afforded access to hexacadmium macrocycles in high yield. These supramolecular assemblies were character
Formylation and dichloromethylation as alternative directions of rieche reaction. A novel to the synthesis of sterically hindered aromatic dialdhydes
Yakubov, Alexander P.,Tsyganov, Dmitry V.,Belen'kii, Leonid I.,Krayushkin, Mikhail M.
, p. 3397 - 3404 (2007/10/02)
A previously unknown direction of Rieche reaction has been found: formylation of mesitylene, m-xylene, and durene with dichloromethyl methyl ether in the presence of aluminium trichloride and, to lesser extent, of titanium tetrachloride give the respective benzylidene dichlorides besides aldehydes. A novel approach to the synthesis of sterically hindered aromatic dialdehydes has been offered which involves the transformation of a monoaldehyde into the corresponding benzylidene dichloride, Rieche formylation of the latter, and hydrolysis of dichloromethyl aldehyde formed.
SYNTHESIS OF STERICALLY HINDERED AROMATIC ALDEHYDES
Yakubov, A. P.,Tsyganov, D. V.,Belen'kii, L. I.,Krayushkin, M. M.
, p. 1427 - 1432 (2007/10/02)
Formylation of mesitylene, durene, and m-xylene derivatives containing electron-donor and electron-acceptor substituents by dichloromethyl methyl ether was studied in the presence of TiCl4.A series of functionally substituted sterically hindered benzaldehydes was prepared from the products of these reactions.