Regioselective Synthesis of 3,3-Diethyl-4-(methylene)-1-quinol-2-ones by an Intramolecular Microwave Assisted Heck Reaction.

ChemInform ◽  
2005 ◽  
Vol 36 (33) ◽  
Author(s):  
Terrence L. Jr. Smalley ◽  
Wendy Y. Mills
Keyword(s):  
Heck Reaction ◽  
Regioselective Synthesis ◽  
Microwave Assisted

A Practical Route to a Complex Bis-Steroidal Diene Intermediate Using a Microwave Assisted Heck-Reaction

Synthesis ◽  
2002 ◽  
pp. 1373-1378 ◽  
Author(s):  
E. Winterfeldt ◽  
T. Flessner ◽  
V. Ludwig ◽  
H. Siebeneicher
Keyword(s):  
Heck Reaction ◽  
Microwave Assisted

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

ChemInform Abstract: Microwave-Assisted Asymmetric Intermolecular Heck Reaction Using Phosphine-Thiazole Ligands.

ChemInform ◽  
2008 ◽  
Vol 39 (15) ◽  
Author(s):  
Paivi Kaukoranta ◽  
Klas Kaellstroem ◽  
Pher G. Andersson
Keyword(s):  
Heck Reaction ◽  
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.

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