Three-Component Reaction between Alkynes, Elemental Sulfur, and Aliphatic Amines: A General, Straightforward, and Atom Economical Approach to Thioamides

2013 ◽  
Vol 16 (1) ◽  
pp. 310-313 ◽  
Author(s):  
Thanh Binh Nguyen ◽  
Minh Quan Tran ◽  
Ludmila Ermolenko ◽  
Ali Al-Mourabit
2019 ◽  
Vol 15 ◽  
pp. 1523-1533 ◽  
Author(s):  
András György Németh ◽  
György Miklós Keserű ◽  
Péter Ábrányi-Balogh

A new multicomponent reaction has been developed between isocyanides, sulfur and alcohols or thiols under mild reaction conditions to afford O-thiocarbamates and dithiocarbamates in moderate to good yields. The one-pot reaction cascade involves the formation of an isothiocyanate intermediate, thus a catalyst-free synthesis of isothiocyanates, as valuable building blocks from isocyanides and sulfur is proposed, as well. The synthetic procedure suits the demand of a modern organic chemist, as it tolerates a wide range of functional groups, it is atom economic and easily scalable.


2012 ◽  
Vol 34 (3) ◽  
pp. 227-232 ◽  
Author(s):  
Alexander V. Artem'ev ◽  
Svetlana F. Malysheva ◽  
Nataliya A. Belogorlova ◽  
Nina K. Gusarova

2012 ◽  
Vol 14 (23) ◽  
pp. 5948-5951 ◽  
Author(s):  
Thanh Binh Nguyen ◽  
Ludmila Ermolenko ◽  
William A. Dean ◽  
Ali Al-Mourabit

2021 ◽  
Vol 36 (1) ◽  
pp. 323-327
Author(s):  
Elaheh Madadi

N-Methyl imidazolium acetate [HMIm]OAc was simply prepared through reaction of N-methyl imidazole with acetic acid and it was applied as a media and promoter for Strecker synthesis of α-aminonitriles. The three component reaction of a variety of structurally different aldehydes and amines with trimethylsilyl cyanide (TMSCN) in the presence of [HMIm]OAc were evaluated. Reaction of aromatic aldehydes and cinnamaldehyde with either aromatic and aliphatic amines provided the corresponding α-aminonitriles in high to excellent isolated yields after short period of time at room temperature.


Synthesis ◽  
2021 ◽  
Author(s):  
Di Ke ◽  
You Wu ◽  
Lei Zhang ◽  
Jiaan Shao ◽  
Yongping Yu ◽  
...  

A group-assisted-purification (GAP) chemistry strategy based Ugi four-center three-component reaction (Ugi-4C-3CR) was explored. The reaction proceeded well to deliver the cyclic fused pyridinones selectively. Moreover, the reaction condition was mild and avoided additional chromatography or recrystallization work-up. Also, wide variations in substrates, such as anilines and aliphatic amines as well as amino alcohols and amino acid esters were all tolerated and achieved in good to excellent yields. Importantly, ladder-type cyclic fused pyridinones can be further constructed with excellent yield of 91%.


Sign in / Sign up

Export Citation Format

Share Document