Furan derivatives. XL. Synthesis of 5-nitro-2-substituted furans on the basis of 5-nitrofurfuryl nitrate

1972 ◽  
Vol 37 (9) ◽  
pp. 3144-3147 ◽  
Author(s):  
A. Jurášek ◽  
J. Kováč ◽  
A. Krutošíková ◽  
M. Hrdina
2019 ◽  
Vol 55 (58) ◽  
pp. 8394-8397 ◽  
Author(s):  
Jie Hu ◽  
Youwen Fei ◽  
Hongbin Zhao ◽  
Zhishuang Wang ◽  
Chunju Li ◽  
...  

A novel rearrangement of ester-activated propargylic acetate with isocyanide has been disclosed. This protocol enables a quick synthesis of polysubstituted furan derivatives.


2015 ◽  
Vol 2 (1) ◽  
pp. 47-50 ◽  
Author(s):  
Wen-Biao Zhang ◽  
Shi-Dong Xiu ◽  
Chuan-Ying Li

The efficient synthesis of highly functionalized furan derivatives from 1-sulfonyl-1,2,3-triazoles with a pendent carbonyl group is reported. The process involves an intramolecular trapping of α-imino carbene and subsequent aromatization.


RSC Advances ◽  
2016 ◽  
Vol 6 (40) ◽  
pp. 33462-33467 ◽  
Author(s):  
Soumen Payra ◽  
Arijit Saha ◽  
Sandip Guchhait ◽  
Subhash Banerjee

Here, we have reported CuO nanoparticles catalyzed synthesis of poly-functionalized furan derivatives via direct functionalization of α,β-unsaturated carbonyl compounds through conjugate addition initiated domino reactions in aqueous ethanol.


2010 ◽  
Vol 75 (3) ◽  
pp. 299-305 ◽  
Author(s):  
Hassan Ghasemnejad-Bosra ◽  
Mohammad Faraje ◽  
Setareh Habibzadeh ◽  
Farhad Ramzanian-Lehmali

N-Bromosuccinimide was found to efficiently catalyze the synthesis of highly functionalized, tetra-substituted furan derivatives in the one-pot reactions of but-2-ene-1,4-diones and acetoacetate esters in the presence of i-PrOH as solvent under mild and neutral conditions at 80-90?C for 3-7 h in high yields (87-94%).


1970 ◽  
Vol 48 (10) ◽  
pp. 1550-1553 ◽  
Author(s):  
Hugh J. Anderson ◽  
C. W. Huang

The Friedel–Crafts t-butylation of methyl 2-pyrrolecarboxylate and of 2-acetylpyrrole have been investigated. The results are found to be consistent with the mechanistic pathway suggested in earlier isopropylation papers. Evidence is presented that alkylation of similarly substituted furans may be interpreted in the same way.


2001 ◽  
Vol 42 (34) ◽  
pp. 5841-5844 ◽  
Author(s):  
Timothy J Donohoe ◽  
Jean-Baptiste Guillermin ◽  
Andrew A Calabrese ◽  
Daryl S Walter

ChemInform ◽  
1989 ◽  
Vol 20 (22) ◽  
Author(s):  
O. M. NEFEDOV ◽  
A. E. VASIL'VITSKII ◽  
V. L. ZLATKINA ◽  
D. S. YUFIT ◽  
YU. T. STRUCHKOV ◽  
...  

1993 ◽  
Vol 23 (18) ◽  
pp. 2593-2597 ◽  
Author(s):  
M. Venugopal ◽  
B. Balasundaram ◽  
P. T. Perumal
Keyword(s):  

RSC Advances ◽  
2017 ◽  
Vol 7 (17) ◽  
pp. 10524-10528 ◽  
Author(s):  
Pulaganti Vijayaprasad ◽  
Avudoddi Venkanna ◽  
Medi Shanker ◽  
Eslavath Kishan ◽  
Pallapothula Venkateswar Rao

A simple, efficient and novel methodology has been developed for the synthesis of substituted furans mediated by triflic acid. In the reaction initial step involves the Friedel–Crafts arylation, followed by the dehydrative cyclization.


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