Direct and facile synthesis of acyl azides from carboxylic acids using the trichloroisocyanuric acid–triphenylphosphine system

2013 ◽  
Vol 91 (3) ◽  
pp. 181-185 ◽  
Author(s):  
Batool Akhlaghinia ◽  
Hamed Rouhi-Saadabad

A mild, efficient, and practical method for the one-step synthesis of acyl azides from carboxylic acids using a safe and inexpensive mixed reagent, trichloroisocyanuric acid–triphenylphosphine, is described.

2009 ◽  
Vol 7 (4) ◽  
pp. 818-826 ◽  
Author(s):  
Tuula Kylmälä ◽  
Jan Tois ◽  
Youjun Xu ◽  
Robert Franzén

AbstractDiflunisal and Felbinac, two FDA-approved NSAIDs and other biphenyl carboxylic acids were prepared in one step by a simple and clean Suzuki cross-coupling reaction using an easily synthesized, air and moisture stable, palladium-diamine complex. The yield (93%) for the one-step preparation of Diflunisal is the best reported without using a glovebox and a phoshine-based catalyst.


2019 ◽  
Author(s):  
Arthur Bonfá Fernandes ◽  
Mariia V. Pavliuk ◽  
Cristina Paun ◽  
Alexandrina C. Carvalho ◽  
Cassiana S. Nomura ◽  
...  

Metal nanoparticles have been widely exploited in catalysis, but their full impact on the environment and human health is still under debate. Here we describe the one-step fabrication of polymer microbead-supported metal and metal oxide nanoparticles and their application as recoverable nanocatalysts for reactions under batch and flow conditions. Au, Ag and Fe<sub>3</sub>O<sub>4</sub> nanoparticles were prepared directly at the surface of benzylamine-coated spherical polymer beads in water by using low energy microwave radiation. The morphology and size of the nanoparticles, and therefore their catalytic properties, were tuned by modifying the bead surface using betalamic acid, an antioxidant from plant origin. The catalytic performance and recovery of these environmentally friendly nanocatalysts was demonstrated towards model redox chemical transformations. We anticipate the results reported herein can provide important insights into the controlled and facile synthesis of microparticle supported nanocatalysts under mild conditions.


1975 ◽  
Vol 30 (7-8) ◽  
pp. 606-608 ◽  
Author(s):  
H. A. B. Linke ◽  
D. E. Eveleigh

The flavanone glycosides naringin, neohesperidin and hesperidin were converted chemically to the corresponding chalcones and dihydrochalcones; the one-step synthesis, performed at room temperature, required the presence of 25% KOH in the reaction mixture for the former and 10% KOH, a catalyst and molecular hydrogen at atmospheric pressure for the latter.


2021 ◽  
Author(s):  
Chi Yang ◽  
Tian-Rui Wu ◽  
Yan Li ◽  
Bing-Bing Wu ◽  
Ruo-Xing Jin ◽  
...  

Palladium-catalyzed asymmetric C–H functionalization to yield axially chiral styrene-type carboxylic acids is described, in which axial chirality and sterically hindered group were incorporated in one-step.


2017 ◽  
Vol 19 (23) ◽  
pp. 5591-5598 ◽  
Author(s):  
Xing Liu ◽  
Min Liu ◽  
Wan Xu ◽  
Meng-Tian Zeng ◽  
Hui Zhu ◽  
...  

An efficient and practical method for the one-step synthesis of benzothiazole-2-thiols, benzoxazole-2-thiols and benzimidazoline-2-thiones in water was described.


Synlett ◽  
2020 ◽  
Vol 31 (14) ◽  
pp. 1413-1417
Author(s):  
Chengrong Ding ◽  
Guofu Zhang ◽  
Lidi Xuan ◽  
Yiyong Zhao

A novel SO2F2-promoted thiocyanation method for the one-step synthesis of thiocyanates through C–O bond cleavage of readily available alcohols with ammonium thiocyanate as the thiocyanating agent was developed. The method avoids the use of additional catalyst, and a variety of (hetero)arene, alkene and aliphatic alcohols reacted with high efficiency in ethyl acetate under mild conditions to afford the corresponding thiocyanates in excellent to quantitative yields with broad functional-group compatibility.


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