Water‐Promoted Synthesis of Azepino[3,4,5‐ cd ]indole Analogues via Pictet‐Spengler Reaction

2020 ◽  
Vol 5 (15) ◽  
pp. 4619-4622
Author(s):  
Shuaizhong Zhang ◽  
Yunrui Cai ◽  
Hongbin Zou
Keyword(s):  
2011 ◽  
Vol 21 (11) ◽  
pp. 3809-3817 ◽  
Author(s):  
Saundane Anand Raghunath ◽  
Yarlakatti Manjunatha ◽  
Kalpana Rayappa

2013 ◽  
Vol 5 (4) ◽  
pp. 275-280 ◽  
Author(s):  
V. Lakshmi Ranganatha ◽  
A. Bushra Begum ◽  
T. Prashanth ◽  
H.D. Gurupadaswamy ◽  
S.K. Madhu ◽  
...  

Tetrahedron ◽  
2007 ◽  
Vol 63 (25) ◽  
pp. 5379-5385 ◽  
Author(s):  
Zoe E. Wilson ◽  
Amanda M. Heapy ◽  
Margaret A. Brimble

1996 ◽  
Vol 36 (4) ◽  
pp. 664-671 ◽  
Author(s):  
A. E. Medvedev ◽  
A. S. Ivanov ◽  
A. V. Veselovsky ◽  
V. S. Skvortsov ◽  
A. I. Archakov

2009 ◽  
Vol 17 (13) ◽  
pp. 4583-4594 ◽  
Author(s):  
Christian Markl ◽  
Mohamed I. Attia ◽  
Justin Julius ◽  
Shalini Sethi ◽  
Paula A. Witt-Enderby ◽  
...  

2014 ◽  
Vol 2014 ◽  
pp. 1-8 ◽  
Author(s):  
Jaiprakash S. Biradar ◽  
Parveen Rajesab ◽  
Sasidhar B. Somappa

We describe herein the design, synthesis, and pharmacological evaluation of novel series of imidazolopyridinyl indole analogues as potent antioxidants and antimicrobials. These novel compounds (3a–i) were synthesized by reacting 3,5-disubstituted-indole-2-carboxylic acid (1a–i) with 2,3-diamino pyridine (2) in excellent yield. The novel products were confirmed by their IR,1H NMR,13C NMR, mass spectral, and analytical data. These compounds were screened for their antioxidant and antimicrobial activities. Among the compounds tested,3a–dshowed the highest total antioxidant capacity, scavenging, and antimicrobial activities. Compounds3c-dand3g-hhave shown excellent ferric reducing activity.


Sign in / Sign up

Export Citation Format

Share Document