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6,7-Dihydro- -1-oxid

Benz[a]acridine-3,4-diol, 3,4-dihydro-oxidation, 2, 184-185 Benz[c]acridine-3,4-diol, 3,4-dihydro-oxidation, 2, 185 Benzacri dines synthesis... [Pg.533]

Benzothiazole, 2-amino-6-thiocyanato-azo dyes from, 1, 328 Benzothiazole, 2-aryl-synthesis, 6, 321 Benzothiazole, 2-arylamino-synthesis, 6, 323 Benzothiazole, 2-aryloxy-Fries rearrangement, 6, 289 Benzothiazole, 2-benzyl-picrate, 6, 252 Benzothiazole, 2-chloro-dyes from, 1, 321-322 synthesis, 6, 323 Benzothiazole, 2,3-dihydro-oxidation, 6, 272 Benzothiazole, 2-dimethylamino-synthesis, 5, 128... [Pg.556]

Grignard reagent, 7, 514 5H-Dibenz[6,/]azepine, 3-chloro-10,l 1-dihydro-oxidation, 7, 525... [Pg.599]

H-Dibenz[c,e]azepine, N-alkyl-6,7-dihydro-oxidation, 7, 511 6H-Dibenz[c,e]azepine, dihydroconformation, 7, 499... [Pg.599]

Pteridin-6-one, 2-chloro-7,8-dihydro-reduction, 3, 293 Pteridin-6-one, 7,8-dihydro-oxidation, 3, 307 structure, 3, 279 Pteridin-6-one, 7-methyl-2,4-disubstituted synthesis, 3, 310 hydroxylation, 3, 287... [Pg.755]

Pyrazine, 2,5-dichloro-3,6-difluoro-synthesis, 3, 190-191 Pyrazine, dihydro-, 3, 177 Pyrazine, 1,2-dihydro-oxidation, 3, 178 reduction, 3, 177 Pyrazine, 1,4-dihydro-antiaromaticity, 3, 177-178 synthesis, 3, 177 Pyrazine, 2,3-dihydro-oxidation, 3, 178 Pyrazine, 2,5-dihydro-synthesis, 3, 178 Pyrazine, 3,6-dihydro-synthesis, 3, 184 Pyrazine, 2,5-dihydroxy-oxidation, 3, 175 Pyrazine, 2,3-dimethyl-1,4-dioxide... [Pg.768]

Pyrrolo[3,4-6]quinoxaline, 2-/-butyl-1,3-dihydro-oxidation, 4, 509 Pyrrolo[3,2-d Jselenazoles synthesis, 6, 344, 1009... [Pg.824]

The known redox roles of tetrahydropterins in biochemistry led Rajagopalan to investigate the redox behavior of the pterin unit of Moco. They titrated Moco within molybdoproteins (XO and SO) with two different oxidants, ferrocyanide and the redox dye dichlorophenol indophenol (DCIP), and obtained unexpected results two electron equivalents of either oxidant produced the spectral signature of a fully oxidized pterin (Scheme 2.1), a result only consistent with the pterin in Moco starting at the dihydro oxidation state rather than the tetrahydro state as initially proposed. The interpretation at the time was that the pterin in Moco, instead of the initially proposed tetrahydropterin structure, was a dihydropterin in an unusual tautomeric form. [Pg.24]

Pyridineacetic acids, conversion to pyridine side-chain carboxylic acids, 422-420 dihydro, oxidation with O2,... [Pg.1239]

See other pages where 6,7-Dihydro- -1-oxid is mentioned: [Pg.544]    [Pg.544]    [Pg.544]    [Pg.544]    [Pg.599]    [Pg.18]    [Pg.38]   


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1.2- Dithiin 1-oxides, dihydro

1.4- Dihydro-2,3-benzoxathiin 3-oxides

2,5-Dihydro-l,2-oxaphosphole-2-oxides

2-Quinolones, 3,4-dihydro-l-hydroxysynthesis via oxidation of tetrahydroquinolines

2.2.3- Trimethyl-1,2-dihydro-1 -quinoxalinol 4-oxide

2.3- Dihydro quinoline-4-oxides

2//-Pyrrole 1-oxide, 3,4-dihydro

3-Oxo-3,4-dihydro- -1-oxid

3.6- Dihydro-1,2-thiazine 1-oxide

4.5- Dihydro-1,2,4-oxadiazoles, oxidation

4.5- Dihydro-l,3-thiazoles, oxidation

9-Nitro-5,6-dihydro- -3-oxid

Bethoxazin (3-Benzo(b)thien-2-yl-5,6-dihydro-l,4,2-oxathiazine 4-oxide)

Dihydro-, oxidation

Dihydro-, oxidation

Dihydro-, oxidation ring contraction

Dihydro-1,4-thiazine 1-oxides synthesis

Dihydro-1,4-thiazines oxidation

Furan, 2,5-dimethoxy-2,5-dihydroSubject allylic oxidation

Furan, 2,5-dimethoxy-2,5-dihydroSubject oxidation

Quinazoline oxides 1,2-dihydro- from

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