ChemInform Abstract: PARTIALLY FLUORINATED HETEROCYCLIC COMPOUNDS. PART 16. PREPARATION OF FURAN DERIVATIVES FROM PENTAFLUOROPHENYL AND HEPTAFLUORO-2-NAPHTHYL PROP-2-YNYL ETHERS WITH AROMATIC COMPOUNDS, AND THE ISOLATION OF HYDROGEN-ABSTRACTION PRODUCTS

1982 ◽  
Vol 13 (15) ◽  
Author(s):  
G. M. BROOKE
1977 ◽  
Vol 165 (2) ◽  
pp. 395-402 ◽  
Author(s):  
J Colby ◽  
D I Stirling ◽  
H Dalton

1. Methane mono-oxygenase of Methylococcus capsulatus (Bath) catalyses the oxidation of various substituted methane derivatives including methanol. 2. It is a very non-specific oxygenase and, in some of its catalytic properties, apparently resembles the analogous enzyme from Methylomonas methanica but differs from those found in Methylosinus trichosporium and Methylomonas albus. 3. CO is oxidized to CO2. 4. C1-C8 n-alkanes are hydroxylated, yielding mixtures of the corresponding 1- and 2-alcohols; no 3- or 4-alcohols are formed. 5. Terminal alkenes yield the corresponding 1,2-epoxides. cis- or trans-but-2-ene are each oxidized to a mixture of 2,3-epoxybutane and but-2-en-1-ol with retention of the cis or trans configuration in both products; 2-butanone is also formed from cis-but-2-ene only. 6. Dimethyl ether is oxidized. Diethyl ether undergoes sub-terminal oxidation, yielding ethanol and ethanal in equimolar amounts. 7. Methane mono-oxygenase also hydroxylates cyclic alkanes and aromatic compounds. However, styrene yields only styrene epoxide and pyridine yields only pyridine N-oxide. 8. Of those compounds tested, only NADPH can replace NADH as electron donor.


1958 ◽  
Vol 36 (6) ◽  
pp. 949-951 ◽  
Author(s):  
Owen H. Wheeler

Polycyclic aromatic compounds can, in a number of cases, be oxidized with chromyl chloride, whereas heterocyclic compounds are unaffected.


2014 ◽  
Vol 472 ◽  
pp. 591-595 ◽  
Author(s):  
Xin Tao Cui ◽  
Yong Fa Zhang ◽  
Dong Liu Dong ◽  
Yu Qiong Zhao

Distillation and GC-MS were employed to analysis the coal tar of low-temperature pyrolysis of lignite briquette by contrasting with standards: the fraction below 340°C in the tar distillates of brown coal tar accounted for 83.30% and the other greater than 340°C is pitch accounted for 16.32%. 34.00% of coal tar are hydrocarbons which are mainly consisted of fat aliphatic hydrocarbon and include few alkene and cycloparaffins. The content of phenolic compounds in coal tar, mainly comes from the fraction below 210°C, is 11.68%. 16.86% of coal tar is aromatic compounds which are mainly composed of substitutive derivative of polyalkylbenzene distributing in all kinds of fractions; and a small amount of aromatic compounds which is concentrated in the fraction below 300°C. The content of oxygen-containing, nitrogen-containing and heterocyclic compounds is 4.47%, 0.57%, 2.11%, respectively.


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