scholarly journals Palladium-Catalyzed Coupling Reaction of Terminal Alkynes with Aryl Iodides in the Presence of Indium Tribromide and Its Application to a One-Pot Synthesis of 2-Phenylindole.

ChemInform ◽  
2004 ◽  
Vol 35 (38) ◽  
Author(s):  
Norio Sakai ◽  
Kimiyoshi Annaka ◽  
Takeo Konakahara
2018 ◽  
Vol 42 ◽  
pp. 63-74 ◽  
Author(s):  
Muhammad ZAFAR ◽  
Sabeen ZAHRA ◽  
Muhammad TAHIR ◽  
Ehsan MUGHAL ◽  
Muhammad NAZAR ◽  
...  

ChemInform ◽  
2012 ◽  
Vol 43 (9) ◽  
pp. no-no
Author(s):  
Masafumi Ueda ◽  
Shoichi Sugita ◽  
Naoki Aoi ◽  
Aoi Sato ◽  
Yuki Ikeda ◽  
...  

2003 ◽  
Vol 5 (15) ◽  
pp. 2731-2734 ◽  
Author(s):  
Mariana Bonaterra ◽  
Sandra E. Martín ◽  
Roberto A. Rossi

RSC Advances ◽  
2016 ◽  
Vol 6 (23) ◽  
pp. 19571-19575 ◽  
Author(s):  
Jun Ge ◽  
Xiaojian Wang ◽  
Tianqi Liu ◽  
Zeyu Shi ◽  
Qiong Xiao ◽  
...  

A practical method for one-pot synthesis of substituted phenanthridines is described. Via this method, a series of substituted phenanthridines are obtained in good yields with remarkable functional groups compatibility.


2015 ◽  
Vol 13 (46) ◽  
pp. 11362-11368 ◽  
Author(s):  
Jianan Zhu ◽  
Ying Wei ◽  
Dongqing Lin ◽  
Changjin Ou ◽  
Linghai Xie ◽  
...  

Under very mild conditions, functionalized benzoxaborole derivatives were prepared in good to excellent yields via a palladium-catalyzed Miyaura borylation reaction of readily available unprotected o-bromobenzylalcohols, and bis(pinacolato)diboron (B2pin2) without the assistance of an acid.


RSC Advances ◽  
2016 ◽  
Vol 6 (51) ◽  
pp. 45036-45040 ◽  
Author(s):  
Gajula Raju ◽  
Vijayacharan Guguloth ◽  
Battu Satyanarayana

The catalytic reaction of ketoximes with aryl iodides via a Beckmann rearrangement in the presence of a catalytic amount of Pd(OAc)2, Ag2O and ZnBr2 gave substituted phenanthridines in good to excellent yield.


Sign in / Sign up

Export Citation Format

Share Document