Microwave‐Assisted/Pd‐Catalyzed Domino Synthesis of 2,3,4‐Triiodoanisole from 3‐Anisic Acid: A Superior Substrate for Regioselective Synthesis of 2,3‐Diiodobiphenyls

2020 ◽  
Vol 5 (9) ◽  
pp. 2848-2853
Author(s):  
Raed M. Al‐Zoubi ◽  
Walid K. Al‐Jammal ◽  
Robert McDonald
Keyword(s):  
Regioselective Synthesis ◽  
Microwave Assisted ◽  
Anisic Acid

Microwave-Assisted Regioselective Synthesis of trans-1-Arenesulfonyl-2-ethoxycarbonyl-3-phenylazetidines

2010 ◽  
Vol 40 (11) ◽  
pp. 1631-1638 ◽  
Author(s):  
Sarika Malik ◽  
Upender K. Nadir ◽  
Pramod S. Pandey
Keyword(s):  
Regioselective Synthesis ◽  
Microwave Assisted

scholarly journals Microwave-assisted rapid and regioselective synthesis of N-(alkoxycarbonylmethyl) nucleobases in water

2007 ◽  
Vol 18 (5) ◽  
pp. 1061-1067 ◽  
Author(s):  
Guirong Qu ◽  
Zhiguang Zhang ◽  
Haiming Guo ◽  
Mingwei Geng ◽  
Ran Xia
Keyword(s):  
Regioselective Synthesis ◽  
Microwave Assisted

Microwave-assisted regioselective synthesis of acyclic nucleosides through an alkylating reaction with 2-oxa-1,4-butanediol diacetate

2006 ◽  
Vol 84 (5) ◽  
pp. 819-824 ◽  
Author(s):  
Guirong Qu ◽  
Suhui Han ◽  
Zhiguang Zhang ◽  
Mingwei Geng ◽  
Feng Xue
Keyword(s):  
Reaction Time ◽  
Microwave Irradiation ◽  
Regioselective Synthesis ◽  
Environmental Friendliness ◽  
Short Reaction Time ◽  
Microwave Assisted ◽  
Acyclic Nucleosides ◽  
Green Procedure ◽  
Simple Manipulation

An efficient and green procedure for the synthesis of purine acyclic nucleosides through microwave-assisted alkylation of various purine nucleobases with 2-oxa-1,4-butanediol diacetate in the absence of solvent and catalyst is described. The advantages of using this method include its environmental friendliness, simple manipulation, short reaction time, high regioselectivity, and good yields.Key words: acyclic nucleosides, microwave irradiation, regioselectivity, alkylation, 2-oxa-1,4-butanediol diacetate.

Nano-NiFe2O4 catalyzed microwave assisted one-pot regioselective synthesis of novel 2-alkoxyimidazo[1,2-a]pyridines under aerobic conditions

RSC Advances ◽  
2016 ◽  
Vol 6 (15) ◽  
pp. 12402-12407 ◽  
Author(s):  
Soumen Payra ◽  
Arijit Saha ◽  
Subhash Banerjee
Keyword(s):  
Michael Addition ◽  
Regioselective Synthesis ◽  
Reusable Catalyst ◽  
One Pot ◽  
Aerobic Conditions ◽  
Microwave Assisted ◽  
Ligand Transfer

Here, we have demonstrated regioselective synthesis of novel 2-alkoxy-3-arylimidazo[1,2-a]pyridines using nano-NiFe2O4 as reusable catalyst via one-pot sequential aza-Michael addition, Fe-promoted ligand transfer and C–H imination reactions.

scholarly journals A facile and regioselective multicomponent synthesis of chiral aryl-1,2-mercaptoamines in water followed by monoamine oxidase (MAO-N) enzymatic resolution

2019 ◽  
Vol 17 (40) ◽  
pp. 8982-8986
Author(s):  
Kate Lauder ◽  
Domiziana Masci ◽  
Anita Toscani ◽  
Aya Al Mekdad ◽  
Gary W. Black ◽  
...  
Keyword(s):  
Monoamine Oxidase ◽  
Regioselective Synthesis ◽  
Multicomponent Synthesis ◽  
Enzymatic Resolution ◽  
Microwave Assisted

A microwave assisted multicomponent protocol on water allows the regioselective synthesis of chiral aryl-1,2-mercaptoamines. The enzymatic resolution of the racemates leads to enantioenriched products.

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