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2,5,7,8-tetramethyl-2- structure

MO calculations, 7, 364 Oxetene, 2-isopropylidene-polysubstituted rearrangement, 7, 377 Oxetene, tetramethyl-structure, 7, 366 Oxetenes, 7, 363-402 decomposition, 7, 375 metabolism, 1, 243 molecular dimensions, 7, 366 thermal stability, 7, 370 Oxetenyl anions aromaticity, 7, 371 Oxetenyl cations aromaticity, 7, 371 Oxichlororaphine occurrence, 3, 196 Oxichromic developers in colour photography, 1, 378-379 Oxidation... [Pg.734]

Thiabicyclo[3.1,0]hex-3-ene synthesis, 4, 784 9-Thiabicyclo[3,3. l]nonane 9,9-dioxide bond, angles, 7, 409 - 5-Thiabicyclo-2-pentene, 1,2,3,4-tetrakis(trifiuoromethyl)-rearrangement, 7, 153 2H-l,2-Thiaborin dibenzo fused, 1, 658 1-Thia[2.2.2]cyclazines, 4, 479 5-Thia[2.3.3]cyclazines, 4, 481 Thiacyclobutadienes — see 1H-1A4-Thietes l-Thia-4-cycloheptyne, 3,3,6,6-tetramethyl-structure, 7, 555 synthesis, 7, 574... [Pg.858]

Cyclooctatetraene has two different tetramethyl derivatives with methyl groups on four adja cent carbon atoms They are both completely conjugated and are not stereoisomers Wnte their structures... [Pg.470]

Oxetanone, 3,3,4,4-tetramethyl-solvolysis, 7, 380 2-Oxetanone, 4-trichloromethyl-decarboxylation, 6, 374 dehydrochlorination, 7, 374 structure, 6, 366 2-Oxetanone, 3-trimethylsilyl-synthesis, 7, 395... [Pg.734]

Pteridine, 6-oxo-5,6,7,8-tetrahydro-electrochemistry, 3, 285 Pteridine, 7-oxo-5,6,7,8-tetrahydro-electrochemistry, 3, 285 Pteridine, 2-phenyl-structure, 3, 266 Pteridine, 4-phenyl-structure, 3, 266 Pteridine, 7-phenyl-oxidation, 3, 305 Pteridine, 2,4,6,7-tetraamino-synthesis, 3, 291 Pteridine, 2,4,6,7-tetrabromo-reactions, 3, 291 Pteridine, 2,4,6,7-tetrachloro-hydrolysis, 3, 291 properties, 3, 267 Pteridine, 1,2,3,4-tetrahydro-structure, 3, 280 Pteridine, 5,6,7,8-tetrahydro-reduction, 3, 280 synthesis, 3, 305 Pteridine, 2,4,6,7-tetramethyl-NMR, 3, 266... [Pg.753]

Tetraselenafulvalenes, tetramethyl-Raman spectra, 6, 954, 955 structure, 6, 950 UV spectra, 6, 952 Tetraselenafulvalenes, tetraphenyl-synthesis, 6, 963 1,3,5,7-T etrasilaadamantane formation, 1, 622 Tetrasilabicyclo[3.3. l]octane synthesis, I, 622 T etratellurafulvalenes IR spectra, 6, 954... [Pg.850]

Xanthine, 8-phenyl-synthesis, S, 588 Xanthine, 1,3,8,9-tetramethyl-synthesis, S, 588 Xanthine, 2-thio-dethiation, S, 558 Xanthine, 6-thio-synthesis, S, 588 Xanthine, 1,3,8-trimethyl-synthesis, 3, 308 S, 575 Xanthine, 1,3,9-trimethyl-structure, S, 509 Xanthine, 2,3,8-trimethyl-synthesis, S, 574... [Pg.924]

Structure-activity studies of 5,6,7,8-tetrahdyro-5,5,8,8-tetramethyl-2-quinoxaline derivatives necessitated the preparation of thiophene-containing compound 17. Stetter conditions using thiazolium salt 20 as catalyst resulted in the preparation of 1,4-diketone 21 from 18 and 19. Condensation of 21 with phosphorus pentasulfide followed by saponification resulted in 17. In this fashion, the authors replaced the amide linker of parent compound 22 with the rigid thiophene moiety. [Pg.211]

A recent nuclear magnetic resonance (NMR) study of the structure of 2,3,4,5-tetramethyl, 2,3,4- and 2,3,5-trimethyl, and 2,4-dimethyI-pyrrolium ions in concentrated HCl has shown that they are all protonated on the -carbon and are thus of type (13)... [Pg.292]

Some polymers have both polar and nonpolar groups in the polymer chain. Thermal stability behavior of blends of some such polymers with PVC have also been studied. McNeill and coworkers [149] have studied the degradation of blends of PVC with poly (tetramethyl-ene sebacate) (PTMS). The structure of PTMS is given in Eq. (40). [Pg.332]

The X-ray structure of JV,iV,7,9-tetramethyl-2-phenyl-3//-l,3,4-benzotriazcpin-5- amine shows that the seven-membered ring is severely puckered and that the N1-C2 and N4-C5 bonds possess double-bond character.351... [Pg.462]

Niobium, tetrakis(2,2,6,6-tetramethyl-3,5-heptanedione)-stereochemistry, 1, 94 structure, 1, 93... [Pg.177]

C09-0079. Silicon forms a tetramethyl compound with the formula (0113)4 Si Determine the Lewis structure, determine the shape about each inner atom, and draw a ball-and-stick model of the compound. [Pg.647]

Perhaps chemists will be able to mimic nature without duplicating the iron-sulfur-molybdenum structure. For example, a zirconium complex with tetramethyl cyclopentadiene can bind dinitrogen in a manner that breaks the NON bond, as shown below. Treatment with hydrogen gas results in formation of small amounts of ammonia. Although the yields are too low to make this a viable commercial process, researchers hope to make the process more efficient through chemical modifications and changes in conditions. [Pg.1018]


See other pages where 2,5,7,8-tetramethyl-2- structure is mentioned: [Pg.850]    [Pg.858]    [Pg.881]    [Pg.881]    [Pg.850]    [Pg.881]    [Pg.881]    [Pg.850]    [Pg.881]    [Pg.881]    [Pg.734]    [Pg.850]    [Pg.881]    [Pg.881]    [Pg.423]    [Pg.224]    [Pg.266]    [Pg.851]    [Pg.882]    [Pg.883]    [Pg.163]    [Pg.224]    [Pg.95]    [Pg.153]    [Pg.36]    [Pg.173]    [Pg.282]    [Pg.156]    [Pg.19]    [Pg.68]    [Pg.71]   
See also in sourсe #XX -- [ Pg.480 ]




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