ChemInform Abstract: An Efficient, General Synthesis of 2-Substituted 3,6-Dihydropyrrolo[3,2-e]indoles Involving One-Pot Sonogashira Coupling and Cyclization.

ChemInform ◽  
2013 ◽  
Vol 44 (32) ◽  
pp. no-no
Author(s):  
Moumita Rakshit ◽  
Taraknath Kundu ◽  
Gandhi K. Kar ◽  
Manas Chakrabarty
2017 ◽  
Vol 2017 (27) ◽  
pp. 4026-4034 ◽  
Author(s):  
Mirza Feroz Baig ◽  
Siddiq Pasha Shaik ◽  
Namballa Hari Krishna ◽  
Neeraj Kumar Chouhan ◽  
Abdullah Alarifi ◽  
...  

2003 ◽  
Vol 68 (4) ◽  
pp. 1503-1511 ◽  
Author(s):  
Alexei S. Karpov ◽  
Frank Rominger ◽  
Thomas J. J. Müller
Keyword(s):  

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Xingjie Zhang ◽  
Di Qi ◽  
Chenchen Jiao ◽  
Xiaopan Liu ◽  
Guisheng Zhang

AbstractAlkynes are amongst the most valuable functional groups in organic chemistry and widely used in chemical biology, pharmacy, and materials science. However, the preparation of alkyl-substituted alkynes still remains elusive. Here, we show a nickel-catalyzed deaminative Sonogashira coupling of alkylpyridinium salts. Key to the success of this coupling is the development of an easily accessible and bench-stable amide-type pincer ligand. This ligand allows naturally abundant alkyl amines as alkylating agents in Sonogashira reactions, and produces diverse alkynes in excellent yields under mild conditions. Salient merits of this chemistry include broad substrate scope and functional group tolerance, gram-scale synthesis, one-pot transformation, versatile late-stage derivatizations as well as the use of inexpensive pre-catalyst and readily available substrates. The high efficiency and strong practicability bode well for the widespread applications of this strategy in constructing functional molecules, materials, and fine chemicals.


2019 ◽  
Vol 9 (22) ◽  
pp. 6471-6481 ◽  
Author(s):  
Narasimha Swamy Thirukovela ◽  
Ramesh Balaboina ◽  
Vinayak Botla ◽  
Ravinder Vadde ◽  
Sreekantha Babu Jonnalagadda ◽  
...  

Catalyst efficacy of in situ generated Pd-nanoparticles in the regioselective one-pot synthesis of substituted pyrazoles and isoxazoles via sequential coupling-cyclization methodology in environmentally benign medium is described.


ChemInform ◽  
1989 ◽  
Vol 20 (34) ◽  
Author(s):  
H. G. KRISHNAMURTY ◽  
B. PARKASH ◽  
S. SATHYANARAYANA
Keyword(s):  
One Pot ◽  

2018 ◽  
Vol 42 (5) ◽  
pp. 271-273 ◽  
Author(s):  
Li-fen Peng ◽  
Jia-ying Lei ◽  
Li Wu ◽  
Zi-long Tang ◽  
Zhi-peng Luo ◽  
...  

Me3Si-/Ph2P(O)-protected ethynes were successfully transformed to unsymmetrical arylethynes via a one-pot Ph2P(O)-deprotection/ [Pd(dppf)Cl2]-catalysed coupling and one-pot Me3Si-deprotection/Sonogashira coupling under mild conditions and in high yield. Unsymmetrical phenylethynes, unsymmetrical extended phenylene ethynylenes and unsymmetrical anthrylethynes were successfully synthesised in good to excellent yields.


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