172904-46-0Relevant articles and documents
Syntheses, structures and catalytic activity for Friedel-Crafts reactions of substituted indenyl rhenium carbonyl complexes
Ma, Zhihong,Zhang, Xinli,Wang, Hong,Han, Zhangang,Zheng, Xuezhong,Lin, Jin
, p. 709 - 721 (2017)
The complexes [(η5-C9H6R)Re(CO)3] [R?=?nBu (8), tBu (9), CH(CH2)4 (10), Ph (11), Bz (12), 4-methoxyphenyl (13), 4-chlorophenyl (14)] were synthesized by refluxing substituted indenyl ligands [C9H7R] [R?=?nBu (1), tBu (2), CH(CH2)4 (3), Ph (4), Bz (5), 4-methoxyphenyl (6), 4-chlorophenyl (7)], and Re2(CO)10 in decalin. The molecular structures of 9, 10, 12, and 13 were determined by X-ray diffraction analysis. These four crystals have similar molecular structures of the mononuclear carbonyl complex. In each of these molecules, Re is η5-coordinated to the five-membered ring of the indenyl group. Complexes 8–14 have catalytic activity for Friedel-Crafts reactions of aromatic compounds with a variety of alkylation and acylation reagents. Compared with traditional catalysts, these mononuclear metal carbonyl complexes have obvious advantages such as high activities, mild reaction conditions, high selectivity, and environmentally friendly chemistry.
Palladium-catalyzed benzannulation from alkynes and allylic compounds
Tsukada, Naofumi,Sugawara, Shuichi,Nakaoka, Keiichiro,Inoue, Yoshio
, p. 5961 - 5966 (2007/10/03)
Various alkynes reacted with allyl tosylates in the presence of palladium catalysts, giving polysubstituted benzenes with good to high regioselectivity. Pentasubstituted and trisubstituted benzenes were readily prepared by reaction of internal alkynes and
Benzannulation from alkynes and allyl tosylates via a π-allylpalladium intermediate
Tsukada, Naofumi,Sugawara, Shuichi,Inoue, Yoshio
, p. 655 - 657 (2007/10/03)
(Graph presented) Allyl tosylate is a good allyl source for a novel palladium-catalyzed benzannulation that affords polysubstituted benzenes from 1 mol of an allyl compound and 2 mol of internal alkynes. Using triphenyl phosphite as a ligand, the reaction with terminal alkynes gave trisubstituted benzenes regioselectively.
Rhenium complexes-catalyzed alkylation of arenes with alkyl halides
Nishiyama,Kakushou,Sonoda
, p. 2779 - 2782 (2007/10/03)
Rhenium complexes have been shown to catalyze the alkylation of arenes with alkyl halides. When arenes were reacted with an alkyl chloride in the presence of a catalytic amount of rhenium complexes, such as bromopentacarbonylrhenium(I) [ReBr(CO)5], tricarbonylcyclopentadienylrhenium(I) [Re(C5H5)(CO)3] and decacarbonyldirhenium [Re2(CO)10], alkylation of the arenes proceeded under mild conditions to give a mixture of mono- and dialkyl substituted arenes in moderate-to-good yields.
