scholarly journals Single-step Syznthesis of Coenzyme Q0

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.

2017 ◽  
Vol 2 (17) ◽  
pp. 4963-4968 ◽  
Author(s):  
Abhinandan D. Hudwekar ◽  
G. Lakshma Reddy ◽  
Praveen K. Verma ◽  
Sorav Gupta ◽  
Ram A. Vishwakarma ◽  
...  

2016 ◽  
Vol 3 (9) ◽  
pp. 1096-1099 ◽  
Author(s):  
Huanhuan Liu ◽  
Tianran Zhai ◽  
Shiteng Ding ◽  
Yalei Hou ◽  
Xiangyu Zhang ◽  
...  

New method for synthesis of 2-hetarylquinazolin-4(3H)-ones from 2-aminobenzamides and (2-azaaryl)methanes under transition-metal free conditions, featuring a wide substrate scope with a broad range of functional group tolerance under mild conditions.


Synthesis ◽  
2020 ◽  
Vol 52 (16) ◽  
pp. 2395-2409
Author(s):  
Weiwei Qin ◽  
Zhaodong Li ◽  
Yiming Du ◽  
Yue Chen ◽  
Yun-Lin Liu

An efficient, PhI(OAc)2-mediated, radical azidoheteroarylation of alkenes under transition-metal-free conditions is reported by employing TMSN3 and quinoxalin-2(1H)-ones as coupling partners. This domino reaction allows an efficient synthesis of valuable orangoazides containing quinoxalin-2(1H)-one derivatives and could be extended to phosphinyl-alkylated quinoxalin-2(1H)-one in a single step in moderate to excellent yields under mild conditions, as demonstrated by the preliminary antibacterial evaluation against Magnaporthe grisea for the first time. Mechanistic studies revealed that this transformation undergoes a cascade addition pathway controlled by a polar radical.


2019 ◽  
Vol 17 (40) ◽  
pp. 9014-9025 ◽  
Author(s):  
Abhilash Sharma ◽  
Pranjal Gogoi

A mild, efficient and transition-metal free synthetic strategy has been developed for the α-arylation of 4-aminocoumarins using arynes as an aryl source. This synthetic strategy proceeds via C(sp2)–C(sp2) bond formation between 4-aminocoumarins and aryne precursors in a single step in the absence of a metal-catalyst.


2017 ◽  
Vol 4 (2) ◽  
pp. 232-235 ◽  
Author(s):  
Xia Zhao ◽  
Aoqi Wei ◽  
Tianjiao Li ◽  
Zhiyang Su ◽  
Jun Chen ◽  
...  

A new method for phosphine-mediated difluoromethylthiolation of indoles and other electron-rich aromatics using difluoromethanesulfonyl chloride was developed.


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.


ChemInform ◽  
2015 ◽  
Vol 46 (10) ◽  
pp. no-no
Author(s):  
Meghdad Karimi ◽  
Dariush Saberi ◽  
Kobra Azizi ◽  
Marzban Arefi ◽  
Akbar Heydari

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 ◽  
...  

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>


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

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