Copper-Catalyzed Three-Component One-Pot Synthesis of Aryl Sulfides with Sulfur Powder under Aqueous Conditions

2016 ◽  
Vol 358 (23) ◽  
pp. 3881-3886 ◽  
Author(s):  
Fuhong Xiao ◽  
Shuqing Chen ◽  
Cheng Li ◽  
Huawen Huang ◽  
Guo-Jun Deng
Keyword(s):  
One Pot ◽  
Sulfur Powder ◽  
One Pot Synthesis ◽  
Aqueous Conditions ◽  
Aryl Sulfides

One-Pot Synthesis of Symmetrical and Unsymmetrical Aryl Sulfides by Pd-Catalyzed Couplings of Aryl Halides and Thioacetates

2011 ◽  
Vol 76 (11) ◽  
pp. 4371-4378 ◽  
Author(s):  
Namjin Park ◽  
Kyungho Park ◽  
Mihee Jang ◽  
Sunwoo Lee
Keyword(s):  
Aryl Halides ◽  
One Pot ◽  
One Pot Synthesis ◽  
Aryl Sulfides

One-Pot Synthesis of Amine-Substituted Aryl Sulfides and Benzo[b]thiophene Derivatives

2010 ◽  
Vol 12 (10) ◽  
pp. 2430-2433 ◽  
Author(s):  
Zhongyu Duan ◽  
Sadananda Ranjit ◽  
Xiaogang Liu
Keyword(s):  
One Pot ◽  
One Pot Synthesis ◽  
Thiophene Derivatives ◽  
Aryl Sulfides

A Facile One-Pot Synthesis of Alkyl Aryl Sulfides from Aryl Bromides

2004 ◽  
Vol 69 (9) ◽  
pp. 3236-3239 ◽  
Author(s):  
Jungyeob Ham ◽  
Inho Yang ◽  
Heonjoong Kang
Keyword(s):  
One Pot ◽  
Alkyl Aryl ◽  
One Pot Synthesis ◽  
Aryl Bromides ◽  
Aryl Sulfides

Base-Promoted Three-Component One-Pot Synthesis of 3- (Thiomethyl)indoles with Paraformaldehyde under Aqueous Conditions

Synlett ◽  
2018 ◽  
Vol 29 (20) ◽  
pp. 2693-2696 ◽  
Author(s):  
Fuhong Xiao ◽  
Guo-Jun Deng ◽  
Shanshan Yuan ◽  
Huawen Huang
Keyword(s):  
Carbon Source ◽  
Environmentally Friendly ◽  
Green Solvent ◽  
One Pot ◽  
One Pot Synthesis ◽  
Low Toxicity ◽  
Aqueous Conditions

An ethylenediamine-promoted three-component synthesis of 3-(thiomethyl)indoles from indoles, thiophenols, and paraformaldehyde has been developed. Water is used as the green solvent in a simple and environmentally friendly procedure. Stable and low-toxicity paraformaldehyde is used as a carbon source.

scholarly journals Efficient Cu-catalyzed base-free C–S coupling under conventional and microwave heating. A simple access to S-heterocycles and sulfides

2013 ◽  
Vol 9 ◽  
pp. 467-475 ◽  
Author(s):  
Silvia M Soria-Castro ◽  
Alicia B Peñéñory
Keyword(s):  
Microwave Irradiation ◽  
Microwave Heating ◽  
Catalytic System ◽  
Low Cost ◽  
One Pot ◽  
Alkyl Aryl ◽  
One Pot Synthesis ◽  
Aryl Iodides ◽  
The One ◽  
Aryl Sulfides

S-aryl thioacetates can be prepared by reaction of inexpensive potassium thioacetate with both electron-rich and electron-poor aryl iodides under a base-free copper/ligand catalytic system. CuI as copper source affords S-aryl thioacetates in good to excellent yields, by using 1,10-phenanthroline as a ligand in toluene at 100 °C after 24 h. Under microwave irradiation the time was drastically reduced to 2 h. Both procedures are simple and involve a low-cost catalytic system. This methodology was also applied to the “one-pot” synthesis of target heterocycles, such as 3H-benzo[c][1,2]dithiol-3-one and 2-methylbenzothiazole, alkyl aryl sulfides, diaryl disulfides and asymmetric diaryl sulfides in good yields.

One-pot Synthesis of Benzo[4,5]imidazo[1,2-a]pyridine Derivatives in Aqueous Conditions

2016 ◽  
Vol 54 (1) ◽  
pp. 753-757 ◽  
Author(s):  
Maria A. Vodolazhenko ◽  
Anastasiia E. Mykhailenko ◽  
Nikolay Yu. Gorobets ◽  
Sergey M. Desenko
Keyword(s):  
Pyridine Derivatives ◽  
One Pot ◽  
One Pot Synthesis ◽  
Aqueous Conditions

TBAH-Catalyzed One-Pot Synthesis of Symmetrical Trithiocarbonates from Alkyl Halides and Carbon Disulfide under Neat Aqueous Conditions

Synthesis ◽  
2009 ◽  
Vol 2010 (03) ◽  
pp. 392-394 ◽  
Author(s):  
Mohammad Soleiman-Beigi ◽  
Zeinab Arzehgar ◽  
Barahman Movassagh
Keyword(s):  
Carbon Disulfide ◽  
Alkyl Halides ◽  
One Pot ◽  
One Pot Synthesis ◽  
Aqueous Conditions
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