Regioselective Approach to 5-Carboxy-1,2,3-triazoles Based on Palladium-Catalyzed Carbonylation

Synthesis ◽  
2018 ◽  
Vol 50 (09) ◽  
pp. 1926-1934 ◽  
Author(s):  
Gennadij Latyshev ◽  
Yury Kotovshchikov ◽  
Irina Beletskaya ◽  
Nikolay Lukashev

A regioselective two-step approach to 5-carboxy-1,2,3-triazoles based on palladium-catalyzed carbonylation has been developed. The protocol utilizes readily available 5-iodotriazoles as starting materials. The obtained products were used in the syntheses of fused heterocycles as well as derivatization of the steroidal hormone cortexolone­.

2020 ◽  
Vol 22 (23) ◽  
pp. 9337-9341
Author(s):  
Rong-Shiow Tang ◽  
Li-Yuan Chen ◽  
Chin-Hung Lai ◽  
Ta-Hsien Chuang

RSC Advances ◽  
2014 ◽  
Vol 4 (46) ◽  
pp. 24001-24006 ◽  
Author(s):  
Kommuri Shekarrao ◽  
Partha Pratim Kaishap ◽  
Venkateshwarlu Saddanapu ◽  
Anthony Addlagatta ◽  
Sanjib Gogoi ◽  
...  

An efficient method was developed for the synthesis of pyrazole fused heterocycles via the palladium-catalyzed solvent free reaction of β-halovinyl/aryl aldehydes and 3-aminopyrazoles/5-aminopyrazoles under microwave irradiation in good yields.


2022 ◽  
Author(s):  
Adimurthy Subbarayappa ◽  
Rashmi Semwal ◽  
Gaurav Bhadani

Palladium-catalyzed annulation of imidazo[1,2-a]pyridines with coumarins provided the benzofuran fused transannulated products in good to excellent yields via decarbonylative approach. While imidazo[1,2-a]pyridines with N-methyl indoles in the presence of palladium...


2007 ◽  
Vol 129 (25) ◽  
pp. 7742-7743 ◽  
Author(s):  
Ilya V. Seregin ◽  
Victoria Ryabova ◽  
Vladimir Gevorgyan

2020 ◽  
Vol 11 (1) ◽  
Author(s):  
Fei Ye ◽  
Yao Ge ◽  
Anke Spannenberg ◽  
Helfried Neumann ◽  
Matthias Beller

Abstract There is a continuous need for designing new and improved synthetic methods aiming at minimizing reaction steps while increasing molecular complexity. In this respect, catalytic, one-pot cascade methodologies constitute an ideal tool for the construction of complex molecules with high chemo-, regio-, and stereoselectivity. Herein, we describe two general and efficient cascade procedures for the synthesis of spiro-fused heterocylces. This transformation combines selective nucleophilic substitution (SN2′), palladium-catalyzed Heck and C–H activation reactions in a cascade manner. The use of allylic ammonium salts and specific Pd catalysts are key to the success of the transformations. The synthetic utility of these methodologies is showcased by the preparation of 48 spiro-fused dihydrobenzofuranes and indolines including a variety of fluorinated derivatives.


Synthesis ◽  
2021 ◽  
Author(s):  
Alexander S. Fisyuk ◽  
Sergey A. Chernenko ◽  
Anastasia S. Kostyuchenko ◽  
Anna Samsonenko ◽  
Anton L. Shatsauskas ◽  
...  

A new approach to the synthesis of fused benzothiophene derivatives was developed based on iodine-promoted photo-cyclization of 4,5-diarylsubstituted thiophenes obtained in three steps from commercially available compounds. Comparative analysis showed that photochemical cyclization is a more efficient method for the preparation of fused benzo[b]thiophene derivatives, compared to oxidative coupling 4,5-diarylsubstituted thiophenes in the presence of iron (III) chloride and palladium catalyzed intramolecular arylation. This approach provides an efficient synthesis of functionally substituted naphtho[2,1-b: 3,4-b ']dithiophenes, phenanthro[9,10-b] thiophenes, benzo[1,2-b: 3,4-b': 6 , 5-b '']trithiophenes, as well as new fused heterocycles containing a pyridine ring and / or a carbazole moiety


2017 ◽  
Vol 2 (29) ◽  
pp. 9312-9318 ◽  
Author(s):  
Suresh Kumar Mondal ◽  
Sk Asraf Ali ◽  
Susanta Kumar Manna ◽  
Arabinda Mandal ◽  
Bidyut Kumar Senapati ◽  
...  

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