[4 + 2] Cycloaddition of conjugated azomethines to aryl isothiocyanates and fungitoxicity of the resulting 6,7-dihydro-1,3,4-oxadiazolo[3,2-a]-s-triazine-5-thiones

1988 ◽  
Vol 36 (4) ◽  
pp. 828-831 ◽  
Author(s):  
Lal Dhar S. Yadav ◽  
Atma R. Misra ◽  
Harendra Singh
Keyword(s):  
Aryl Isothiocyanates

scholarly journals Diaminomaleonitrile as a versatile building block for the synthesis of 4,4′-biimidazolidinylidenes and 4,4′-bithiazolidinylidenes

2018 ◽  
Vol 24 (6) ◽  
pp. 303-306
Author(s):  
Mahsa Doomanlou ◽  
Hassan Kabirifard ◽  
Mehdi Asadi ◽  
Maryam Moloudi ◽  
Seyedeh Sara Mirfazli
Keyword(s):  
Building Block ◽  
Ring Closure ◽  
Wide Range ◽  
New Strategy ◽  
Aryl Isocyanates ◽  
Aryl Isothiocyanates

Abstract Ring closure reactions of diaminomaleonitrile (DAMN) with electrophilic aryl isocyanates and aryl isothiocyanates lead to the formation of the target 5,5′-diimino-1,1′-diaryl-4,4′-biimidazolidinylidene-2,2′-diones 2a,b and 2,2′-diarylimino-4,4′-bithiazolidinylidenes 4a–e, respectively. The protocol provides a new strategy for the synthesis of a wide range of alkenes with two electron-donating and two withdrawing substituents of DAMN in moderate to good yields.

New syntheses of aryl isothiocyanates †

1998 ◽  
pp. 889-892 ◽  
Author(s):  
Thierry Besson ◽  
Jérôme Guillard ◽  
Charles W. Rees ◽  
Valérie Thiéry
Keyword(s):  
Aryl Isothiocyanates

One-Pot Synthesis of Thiazolo[3,4-a]Quinoxalines from 1,2-Diamines, Aryl Isothiocyanates and Ethyl Bromopyruvate

2017 ◽  
Vol 41 (12) ◽  
pp. 712-714 ◽  
Author(s):  
Mohammad Piltan
Keyword(s):  
Chromatographic Separations ◽  
One Pot ◽  
One Pot Synthesis ◽  
Three Component Reaction ◽  
Wide Range ◽  
Quinoxaline Derivatives ◽  
First Time ◽  
Aryl Isothiocyanates ◽  
Ethyl Bromopyruvate

Some hitherto unreported thiazolo[3,4- a]quinoxaline derivatives have been synthesised in excellent yields via a one-pot, three-component reaction of benzene-1,2-diamines, ethyl bromopyruvate and aryl isothiocyanates in MeCN, for the first time. The protocol avoids the use of any catalysts or chromatographic separations and provides a wide range of novel thiazolo[3,4- a]quinoxalines.

Sign in / Sign up

Export Citation Format

Share Document