Microwave-Assisted Selective Synthesis of Mono- and Bistriazines with π-Conjugated Spacers and Study of the Optoelectronic Properties

2014 ◽  
Vol 79 (11) ◽  
pp. 4909-4919 ◽  
Author(s):  
A. Ruiz-Carretero ◽  
O. Noguez ◽  
T. Herrera ◽  
J. R. Ramírez ◽  
A. Sánchez-Migallón ◽  
...  
Keyword(s):  
Optoelectronic Properties ◽  
Selective Synthesis ◽  
Microwave Assisted

Selective synthesis of 1,6-anhydro-β-d-mannopyranose and -mannofuranose using microwave-assisted heating

2011 ◽  
Vol 346 (13) ◽  
pp. 1747-1751 ◽  
Author(s):  
Nguyen To Hoai ◽  
Akiyoshi Sasaki ◽  
Masahide Sasaki ◽  
Harumi Kaga ◽  
Toyoji Kakuchi ◽  
...  
Keyword(s):  
Selective Synthesis ◽  
Microwave Assisted

Microwave-Assisted Domino Reactions of Propargylamines with Isothiocyanates: Selective Synthesis of 2-Aminothiazoles and 2-Amino-4-methylenethiazolines

Synlett ◽  
2016 ◽  
Vol 27 (12) ◽  
pp. 1883-1887 ◽  
Author(s):  
Daniele Castagnolo ◽  
Nicoló Scalacci ◽  
Chiara Pelloja ◽  
Marco Radi
Keyword(s):  
Selective Synthesis ◽  
Domino Reactions ◽  
Microwave Assisted

Microwave-Assisted Rapid and Selective Synthesis of cis- and trans-2,4,5-Triarylimidazolines from Aromatic Aldehydes.

ChemInform ◽  
2003 ◽  
Vol 34 (41) ◽  
Author(s):  
Hitoshi Uchida ◽  
Hirofumi Tanikoshi ◽  
Shuichi Nakamura ◽  
Paidi Yella Reddy ◽  
Takeshi Toru
Keyword(s):  
Aromatic Aldehydes ◽  
Selective Synthesis ◽  
Microwave Assisted ◽  
Cis And Trans

Microwave-Assisted Synthesis of Vinyl Esters through Ruthenium-Catalyzed Addition of Carboxylic Acids to Alkynes

2009 ◽  
Vol 62 (3) ◽  
pp. 227 ◽  
Author(s):  
François Nicks ◽  
Lionel Libert ◽  
Lionel Delaude ◽  
Albert Demonceau
Keyword(s):  
Carboxylic Acids ◽  
Efficient Method ◽  
Microwave Assisted Synthesis ◽  
Selective Synthesis ◽  
Terminal Alkynes ◽  
Vinyl Esters ◽  
Microwave Assisted ◽  
Enol Esters

A rapid and efficient method is described for the selective synthesis of enol esters via the microwave-accelerated addition of carboxylic acids to terminal alkynes. The method employs the readily available [RuCl2(p-cymene)(PPh3)] complex as catalyst without the need of bases, and reactions are complete in 20 min.

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