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Furans tetrahydro-

PE, 4. 26 73MI30102, 74MI30100), 587 <73JA291> Furan, tetrahydro-, tin tetrachloride complex dipole moment, 4, 555 B-63MI31000)... [Pg.23]

Benzo[b]furan, 3-(pyrrolidin-1 -yl)-cycloaddition reactions, 4, 636 synthesis, 4, 648 Benzo[b]furan, tetrahydro-synthesis, 4, 671... [Pg.547]

Furan, perfluoro-2-butyltetrahydro-mass spectrometry, 4, 584 Furan, perfluorotetramethyl-synthesis, 4, 676 Furan, 2-phenyl-rotamers, 4, 545 Furan, 3-phenyl-rotamers, 4, 545 synthesis, 4, 663 Furan, 2-styryl-rotamers, 4, 545 Furan, tetraoyano-mass spectrometry, 4, 583 Furan, tetrahydro-applioations, 4, 707 basicity, 4, 554... [Pg.631]

Dibroane Furan, tetrahydro-, compd. with borane (1 1) (8,9) (14044-65-6)... [Pg.243]

Mono(2,6-dimethoxybenzoyl)tartaric acid Butanedioic acid, 2-[(2,6-dimethoxybenzoyl)oxy-3-hydroxy-, [R-(R, R )]- (12) (116212-44-3) 2,6-Dimethoxybenzoic acid Benzoic acid, 2,6-dimethoxy- (8,9) (1466-76-8) Trifluoroadetic anhydride Acetic acid, tritluoro-, anhydride (8,9) (407-25-0) Borane-Tetrahydrofuran Furan, tetrahydro-, compd. with borane (1 1) (8,9) (14044-65-6)... [Pg.48]

Furan, tetrahydro, 2-methyl Sd (roasted) Furan, tetrahydro Sd (roasted) ... [Pg.158]

C4H602, 2-Propenoic acid, methyl ester platinum complex, 26 138 C4H7NO, 3-Butenamide nickel complex, 26 206 C4HsO, Furan, tetrahydro-iron complex, 26 232 magnesium complex, 26 147 neodymium and samarium complexes, 26 20... [Pg.414]

The HDO and isomerization reactions were previously described as bimolecular nucleophilic substitutions with allylic migrations-the so-called SN2 mechanism (7). The first common step is the fixation of the hydride on the carbon sp of the substrate. The loss of the hydroxyl group of the alcohols could not be a simple dehydration -a preliminar elimination reaction- as the 3-butene-l-ol leads to neither isomerization nor hydrodehydroxyl at ion (6). The results observed with vinylic ethers confirm that only allylic oxygenated compounds are able to undergo easily isomerization and HDO reactions. Moreover, we can note that furan tetrahydro and furan do not react at all even at high temperature (200 C). [Pg.292]

DIMETHYL-2-n-PENTYLTETRAHYDROFURAN (Furan, tetrahydro-2,2-dimethyl-6-pentyl-)... [Pg.25]

See other pages where Furans tetrahydro- is mentioned: [Pg.23]    [Pg.23]    [Pg.23]    [Pg.23]    [Pg.23]    [Pg.23]    [Pg.631]    [Pg.130]    [Pg.745]    [Pg.623]    [Pg.16]    [Pg.98]    [Pg.428]    [Pg.118]    [Pg.1080]    [Pg.23]    [Pg.23]    [Pg.23]    [Pg.23]    [Pg.23]    [Pg.23]    [Pg.631]    [Pg.27]   
See also in sourсe #XX -- [ Pg.23 , Pg.88 ]

See also in sourсe #XX -- [ Pg.23 , Pg.88 ]

See also in sourсe #XX -- [ Pg.23 , Pg.88 ]

See also in sourсe #XX -- [ Pg.23 , Pg.88 ]

See also in sourсe #XX -- [ Pg.23 , Pg.88 ]

See also in sourсe #XX -- [ Pg.23 , Pg.88 ]

See also in sourсe #XX -- [ Pg.23 , Pg.88 ]



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Tetrahydro furane

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