CuO/CNTs-catalyzed heterogeneous process: a convenient strategy to prepare furan derivatives from electron-deficient alkynes and α-hydroxy ketones

2012 ◽  
Vol 14 (10) ◽  
pp. 2710 ◽  
Author(s):  
Hua Cao ◽  
Huan-Feng Jiang ◽  
Xiao-Song Zhou ◽  
Chao-Rong Qi ◽  
Yuan-Guang Lin ◽  
...  
Keyword(s):  
Furan Derivatives ◽  
Heterogeneous Process ◽  
Hydroxy Ketones

ChemInform Abstract: CuO/CNTs-Catalyzed Heterogeneous Process: A Convenient Strategy to Prepare Furan Derivatives from Electron-Deficient Alkynes and α-Hydroxy Ketones.

ChemInform ◽  
2013 ◽  
Vol 44 (4) ◽  
pp. no-no
Author(s):  
Hua Cao ◽  
Huan-Feng Jiang ◽  
Xiao-Song Zhou ◽  
Chao-Rong Qi ◽  
Yuan-Guang Lin ◽  
...  
Keyword(s):  
Furan Derivatives ◽  
Heterogeneous Process ◽  
Hydroxy Ketones

On steroids. C. The B-norsteroid hydroxy ketones and their ORD-curves

1966 ◽  
Vol 31 (7) ◽  
pp. 2745-2758 ◽  
Author(s):  
J. Joska ◽  
J. Fajkoš ◽  
F. Šorm
Keyword(s):  
Hydroxy Ketones

A New Method for the Synthesis of Furan Derivatives

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

Oxidation of enamines to α-hydroxy ketones and α-amino ketones using N-sulfonyloxaziridines

1988 ◽  
Vol 29 (35) ◽  
pp. 4365-4368 ◽  
Author(s):  
Franklin A. Davis ◽  
Aurelia C. Sheppard
Keyword(s):  
Hydroxy Ketones

scholarly journals Biodegradation of 5-(Hydroxymethyl)-furfural and Furan Derivatives

Proceedings ◽  
2018 ◽  
Vol 2 (20) ◽  
pp. 1283 ◽  
Author(s):  
María Isabel Igeño ◽  
Rubén Sánchez-Clemente ◽  
Ana G. Población ◽  
M. Isabel Guijo ◽  
Faustino Merchán ◽  
...  
Keyword(s):  
Furan Ring ◽  
Degradation Products ◽  
Chemical Compounds ◽  
Aldehyde Group ◽  
Bacterial Strains ◽  
Fermentation Inhibitors ◽  
Furan Derivatives ◽  
Hydroxymethyl Furfural ◽  
Common Thread ◽  
Lignocellulose Hydrolysates

Furfural and 5-hydroxymethylfurfural (HMF) are degradation products of lignocellulose during pretreatment operations. Furfural compounds are a group of chemical compounds whose common thread is an aldehyde group attached to a furan ring, and they constitute a problem for the development of second-generation biofuels because they act as fermentation inhibitors of the lignocellulose hydrolysates. Up to date, very few bacteria have been described to be able to eliminate them. The objective of this work was to isolate and characterize bacterial strains able to use, as the sole carbon source, 5-(hydroxymethyl)-furfural (HMF) and furan derivatives.

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