Rapid access to indole-fused bicyclo[2.2.2]octanones by merging the umpolung strategy and molecular iodine as a green catalyst

2020 ◽  
Vol 18 (22) ◽  
pp. 4193-4197 ◽  
Author(s):  
Takumi Abe ◽  
Seiya Hirao

We have achieved the one-pot construction of otherwise more difficult to access indole-fused bicyclo[2.2.2]octanones by merging the umpolung strategy and molecular iodine catalyst.

RSC Advances ◽  
2020 ◽  
Vol 10 (66) ◽  
pp. 40508-40513
Author(s):  
Sahar Saadat Hosseinikhah ◽  
Bi Bi Fatemeh Mirjalili ◽  
Naeimeh Salehi ◽  
Abdolahamid Bamoniri

Gum arabic-OPO3H2 (GA-OPO3H2) as a unique natural-based green catalyst was synthesized by the reaction of phosphorus pentoxide with gum arabic.


2020 ◽  
Vol 52 (1) ◽  
pp. 48-55 ◽  
Author(s):  
Afshin Yazdani-Elah-Abadi ◽  
Maliheh Razeghi ◽  
Nasim Shams ◽  
Mehrnoush Kangani ◽  
Razieh Mohebat

2016 ◽  
Vol 24 (2) ◽  
pp. 112-121 ◽  
Author(s):  
Mojtaba Lashkari ◽  
Malek Taher Maghsoodlou ◽  
Mahsa Karima ◽  
Belgais Adrom ◽  
Maryam Fatahpour

Abstract A straightforward, one-pot multicomponent synthesis of 1-(benzothiazolylamino)methyl-2-naphthol derivatives was achieved by condensation of 2-naphthol, aldehydes, and 2- aminobenzothiazole catalyzed by a small amount of citric acid, which acts as a benign enviermentally catalyst. Mild conditions with excellent yields and a simple isolation procedure are noteworthy advantages of this method.


2017 ◽  
Vol 41 (11) ◽  
pp. 673-675 ◽  
Author(s):  
Fahimeh Khazaee Feizabad ◽  
Khatereh Khandan-Barani ◽  
Alireza Hassanabadi

A high-yielding synthesis of 1,2,4,5-tetrasubstituted imidazoles is described, involving the reaction of 1,2-dicarbonyl compounds, aryl aldehydes, amines and ammonium acetate in the presence of a catalytic amount of glutamic acid under thermal, solvent-free conditions. The salient features of this protocol are aerobic conditions, a non-hazardous green catalyst, short reaction times and mild reaction conditions.


2017 ◽  
Vol 15 (39) ◽  
pp. 8410-8417 ◽  
Author(s):  
Ling Chai ◽  
Yuanqing Xu ◽  
Tao Ding ◽  
Xiaomin Fang ◽  
Wenkai Zhang ◽  
...  

The one-pot reaction includes sequential intermolecular addition of thioamides to nitriles, and intramolecular oxidative coupling of N–H and S–H bonds mediated by molecular iodine.


2021 ◽  
Author(s):  
Saideh Rajai-Daryasarei ◽  
Mohammad Hossein Gohari ◽  
Narges Mohammadi

The preparation of heterocyclic compounds has attracted great attention in organic chemistry because of their extensive presence in bioactive molecules, material sciences, and natural products. Accordingly, the straightforward design and...


2011 ◽  
Vol 7 ◽  
pp. 1315-1322 ◽  
Author(s):  
Inhee Cho ◽  
Labros Meimetis ◽  
Lee Belding ◽  
Michael J Katz ◽  
Travis Dudding ◽  
...  

A variety of ortho,ortho'-disubstituted hydrobenzoin derivatives are readily accessible through a directed ortho,ortho'-dimetalation strategy in which the alcohol functions in hydrobenzoin are deprotonated by n-BuLi and the resulting lithium benzyl alkoxides serve as directed metalation groups. The optimization and scope of this reaction are discussed, and the utility of this process is demonstrated in the one-pot preparation of a number of chiral diols as well as a short synthesis of the chiral ligand Vivol.


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