796874-07-2Relevant articles and documents
Transition-Metal-Free Arylation and Alkylation of Diarylmethyl p-Tolyl Sulfones with Zinc Reagents
Miao, Maozhong,Yin, Wenguang,Wang, Lei,Chen, Zhengkai,Xu, Jianfeng,Ren, Hongjun
, p. 10602 - 10612 (2018/09/06)
The transition-metal-free synthesis of unsymmetrical and highly functionalized triarylmethanes through arylation of the situ generated o-QMs from diarylmethyl p-tolyl sulfones with aryl zinc reagents is described. Alkyl zinc reagents are also well tolerated in this reaction. Additionally, the straightforward synthesis of the analogue of the antituberculosis agent A and the key precursor of the anti-breast-cancer agent B are achieved by this strategy.
Diaryloxy methano phenanthrenes: A new class of antituberculosis agents
Panda, Gautam,Shagufta,Mishra, Jitendra Kumar,Chaturvedi, Vinita,Srivastava, Anil K.,Srivastava, Ranjana,Srivastava, Brahm S.
, p. 5269 - 5276 (2007/10/03)
A new series of diaryloxy methano phenanthrenes were prepared through tertiary-aminoalkylations of [(methoxy-phenyl)-phenanthren-9-yl-methyl]-phenols obtained from Friedel-Crafts alkylations on (methoxy-phenyl)-phenanthren-9-yl- methanols. These series of
