Expedient one-step synthesis of nitrogen stilbene analogs by transition metal-free hydroamination of arylacetylenes with pyrroles

Tetrahedron ◽  
2012 ◽  
Vol 68 (7) ◽  
pp. 1963-1971 ◽  
Author(s):  
Marina Yu. Dvorko ◽  
Elena Yu. Schmidt ◽  
Tatyana E. Glotova ◽  
Dmitrii A. Shabalin ◽  
Igor' A. Ushakov ◽  
...  
2020 ◽  
Vol 18 (6) ◽  
pp. 1082-1086 ◽  
Author(s):  
Chunhao Yuan ◽  
Hui Zhang ◽  
Mengna Yuan ◽  
Lei Xie ◽  
Xiaoqun Cao
Keyword(s):  

A novel cyclization of N-alkoxy α-halogenoacetamides with N-sulfonyl-1-aza-1,3-butadienes has been developed for the efficient preparation of 1,4-diazepinones in one step under transition metal-free conditions.


2021 ◽  
Author(s):  
Lucas Pages ◽  
Sebastien Lemouzy ◽  
Marc Taillefer ◽  
Florian Monnier

A Brønsted acid-mediated addition of (hetero)aryl and (cyclo)alkyl sodium sulfinates to <i>N</i>-allenyl derivatives is described under very smooth conditions. This reaction provided a practical and efficient protocol for the synthesis of allylic sulfones in an atom- and step-economic fashion. In addition, an one-step double hydrosulfonylation has also been demonstrated, affording the corresponding 1,3-disulfone in to good yield.<br>


Author(s):  
Yi-Yu Yan ◽  
Yong-Fu Qiu ◽  
Tian-Li Zhang ◽  
Yu-Bei He ◽  
Shi Qi ◽  
...  

A new method for the preparation of 2-methyl-5,6-dimethoxy-1,4-benzoquinone (Coenzyme Q0) was developed. This improved process in one step by the oxidation of 3,4,5-trimethoxytoluene to coenzyme Q0 by simple oxidation using potassium or ammonium persulfate under transition -metal free conditions.


2019 ◽  
Vol 84 (7) ◽  
pp. 4458-4466 ◽  
Author(s):  
Xianzhu Zeng ◽  
Yongliang Tu ◽  
Zhenming Zhang ◽  
Changming You ◽  
Jiao Wu ◽  
...  
Keyword(s):  

2015 ◽  
Vol 51 (33) ◽  
pp. 7180-7183 ◽  
Author(s):  
Dan Zhu ◽  
Denghu Chang ◽  
Lei Shi

A novel transition-metal-free method for the one-step synthesis of thiocyanates via the C–S bond cleavage of readily available thioethers was developed.


ChemInform ◽  
2012 ◽  
Vol 43 (27) ◽  
pp. no-no
Author(s):  
Marina Yu. Dvorko ◽  
Elena Yu. Schmidt ◽  
Tatyana E. Glotova ◽  
Dmitrii A. Shabalin ◽  
Igor' A. Ushakov ◽  
...  

Synthesis ◽  
2020 ◽  
Vol 52 (17) ◽  
pp. 2541-2550
Author(s):  
Zi-Ning Cui ◽  
Ri-Yuan Tang ◽  
Yong-Chao Gao ◽  
Zi-Hao Huang ◽  
Zhao-Sheng Zhang ◽  
...  

A transition-metal-free sulfite-promoted three-component C–H sulfuration between imidazoheterocycles, elemental sulfur, and bromofluoroacetate is developed. Sulfites, including Na2S2O4, NaHSO3, and Na2S2O3, are able to promote the formation of two C–S bonds in one step using elemental sulfur as a green sulfurating agent, allowing the rapid introduction of the synthetically useful S-fluoroacetate group into imidazoheterocycles. These new imidazoheterocycle derivatives bearing an S-fluoroacetate group can be easily modified to produce pharmaceutically attractive compounds.


Author(s):  
Na Luo ◽  
Zhen-Wei Sun ◽  
Xing-Xin Xu ◽  
Xiao-Qiang Hu ◽  
Feng-Cheng Jia

A one-step, transition-metal-free, base-promoted cascade reaction of 2-halogenated arylglyoxals with 2-oxindoles is reported herein, which provides a straightforward approach to structurally diverse free (NH)-indeno[2,1-b]indol-6(5H)-ones in satisfactory yields. Control experiments indicated...


2021 ◽  
Author(s):  
Lucas Pages ◽  
Sebastien Lemouzy ◽  
Marc Taillefer ◽  
Florian Monnier

A Brønsted acid-mediated addition of (hetero)aryl and (cyclo)alkyl sodium sulfinates to <i>N</i>-allenyl derivatives is described under very smooth conditions. This reaction provided a practical and efficient protocol for the synthesis of allylic sulfones in an atom- and step-economic fashion. In addition, an one-step double hydrosulfonylation has also been demonstrated, affording the corresponding 1,3-disulfone in to good yield.<br>


2020 ◽  
Vol 7 (21) ◽  
pp. 3515-3520
Author(s):  
Wubing Yao ◽  
Jiali Wang ◽  
Aiguo Zhong ◽  
Shiliang Wang ◽  
Yinlin Shao

The selective catalytic reduction of amides to value-added amine products is a desirable but challenging transformation.


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