572-45-2Relevant articles and documents
The C-H Activation/Bidirecting Group Strategy for Selective Direct Synthesis of Diverse 1,1′-Biisoquinolines
Kong, Xiangfei,Li, Shiqing,Lv, Hongxu,Xie, Rongrong,Ye, Xiuqing,Yu, Yu
supporting information, p. 4207 - 4212 (2020/06/24)
Multidentate ligands are highly important but difficult to access. Herein we disclose an atom- and step-economic synthesis of highly substituted 1,1′-biisoquinolines by a C-H activation/bididirecting group strategy. Through rational design of a bididirecting group to "N-OH + N-OAc", selective unsymmetrical diannulation with two different alkynes in a one-pot reaction has been achieved for the first time to access unsymmetrical biisoquinolines. Moreover, the resultant biisoquinolines show tunable photoluminescence and serve as aggregation-induced emission (AIE) systems.
Dioximes as synthons for medium ring heterocyclic compounds
Singh, Maya Shankar,Singh, Ashwani Kumar
, p. 851 - 859 (2007/10/03)
A simple and convenient synthetic approach to eight-, nine- and ten- membered nitrogen and oxygen containing heterocycles has been developed. 3,4- Diaryl-1,6,2,5-dioxadiazocines, (3) and (4), 3,4-diaryl-1,6,2,5- dioxadiazonines,(5) and 3,4-diaryl-1,6,2,5-