ChemInform Abstract: Efficient Synthesis of Indole Derivatives via Tandem Cyclization Catalyzed by Magnetically Recoverable Palladium/Magnetite (Pd-Fe3O4) Nanocrystals.

ChemInform ◽  
2016 ◽  
Vol 47 (36) ◽  
Author(s):  
Jungmin Kwon ◽  
Jooyoung Chung ◽  
Sangmoon Byun ◽  
B. Moon Kim
Keyword(s):  
Indole Derivatives ◽  
Efficient Synthesis ◽  
Tandem Cyclization

I2/TBHP-Mediated tandem cyclization and oxidation reaction: Facile access to 2-substituted thiazoles and benzothiazoles

2019 ◽  
Vol 17 (2) ◽  
pp. 252-256 ◽  
Author(s):  
Li Liu ◽  
Chen Tan ◽  
Rong Fan ◽  
Zihan Wang ◽  
Hongguang Du ◽  
...  
Keyword(s):  
Oxidation Reaction ◽  
Efficient Synthesis ◽  
Tandem Cyclization

The efficient synthesis of 2-substituted thiazoles and benzothiazoles has been accomplished employing readily available cysteine esters and 2-aminobenzenethiols as N and S sources.

ChemInform Abstract: CuBr-Promoted Tandem Cyclization/Trifluoromethylation of 2-Alkynylanilines: Efficient Synthesis of 3-Trifluoromethylindoles.

ChemInform ◽  
2015 ◽  
Vol 46 (8) ◽  
pp. no-no
Author(s):  
Guangcun Ge ◽  
Xiaojun Huang ◽  
Changhua Ding ◽  
Hao Li ◽  
Shili Wan ◽  
...  
Keyword(s):  
Efficient Synthesis ◽  
Tandem Cyclization

Selenium‐Mediated Cyclization Reaction of 2‐Vinylanilines with/without Isonitriles: Efficient Synthesis of 2‐Aminoquinoline/ 3‐Aryl‐1 H ‐indole Derivatives

2020 ◽  
Vol 9 (4) ◽  
pp. 588-592 ◽  
Author(s):  
Xi Zhang ◽  
Yong‐Qing Wang ◽  
Anwar L. Alduma ◽  
Ullah Arif S. H ◽  
Xi‐Cun Wang ◽  
...  
Keyword(s):  
Cyclization Reaction ◽  
Indole Derivatives ◽  
Efficient Synthesis

scholarly journals Facile Iodine-Catalyzed Michael Addition of Indoles to α,α′-Bis(arylmethylene)cyclopentanones: An Efficient Synthesis of E-2-(3-Indolylphenylmethyl)-5-phenylmethylenecyclopentanones

2012 ◽  
Vol 2012 ◽  
pp. 1-6 ◽  
Author(s):  
Rammohan Pal ◽  
Arpita Das Gupta ◽  
Asok K. Mallik
Keyword(s):  
Michael Addition ◽  
Good Yield ◽  
Indole Derivatives ◽  
Efficient Synthesis ◽  
Michael Adducts

Iodine-catalyzed reaction of indoles with α,α′-bis(arylmethylene)cyclopentanones afforded one diastereomer of the corresponding Michael adducts, namely, E-2-(3-indolylphenylmethyl)-5-phenylmethylenecyclopentanones, in a good yield. The products form a new group of indole derivatives.

Sequential substitution/ring cleavage/addition reaction of 1-(cyclohex-1-enyl)-piperidine and -pyrrolidine with chloropyruvates for the efficient synthesis of substituted 4,5,6,7-tetrahydro-1H-indole derivatives

Tetrahedron ◽  
2015 ◽  
Vol 71 (48) ◽  
pp. 9143-9153 ◽  
Author(s):  
Vakhid A. Mamedov ◽  
Elena A. Hafizova ◽  
Anastasiya I. Zamaletdinova ◽  
Il'dar Kh. Rizvanov ◽  
Alla B. Mirgorodskaya ◽  
...  
Keyword(s):  
Addition Reaction ◽  
Ring Cleavage ◽  
Indole Derivatives ◽  
Efficient Synthesis
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