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Thiophene opening

Benzo[Z)]thiophene reacts with dimethyl l,2,4,5-tetrazine-3,6-dicarboxylate in a cyclo-addition-fragmentation reaction to yield (143), whereas benzo[A]furan and N- methylindole yield products (144) arising from ring opening and recyclization (76AP679). [Pg.69]

Benzo[6]thiophene, 4,7-dialkoxy-synthesis, 4, 930 Benzo[6]thiophene, 2,3-dialkyl-synthesis, 4, 877-878 Benzo[6]thiophene, 3 -(dialkylamino)-synthesis, 4, 925 Benzo[c]thiophene, 1,3-diaryl-oxidative ring opening, 4, 768 Benzo[6]thiophene, 2,3-dibromo-reactions, 4, 830... [Pg.560]

Benzo[c]thiophene, 1,3-diphenyl-oxidative ring opening, 4, 768 synthesis, 4, 141-142... [Pg.561]

Thiophene, 2-amino-3-cyano-5-phenyl-synthesis, 4, 888-889 Thiophene, 3-amino-4,5-dihydro-cycloaddition reactions, 4, 848 Thiophene, 2-amino-3-ethoxycarbonyl-ring opening, 4, 73 Thiophene, 2-amino-5-methyl-synthesis, 4, 73 Thiophene, 2-anilino-synthesis, 4, 923-924 Thiophene, aryl-synthesis, 4, 836, 914-916 Thiophene, 2-(arylamino)-3-nitro-synthesis, 4, 892 Thiophene, azido-nitrenes, 4, 818-820 reactions, 4, 818-820 thermal fragmentation, 4, 819-820 Thiophene, 3-azido-4-formyl-reactions... [Pg.890]

Thiophene, 2,5-dimethyl-3-lithio-ring opening, 4, 81 Thiophene, 2,5-dimethylthio-3,4-disubstituted synthesis, 4, 872 Thiophene, dinitro-... [Pg.891]

R" = H, R = H) gives similar butadienethiolate complexes. Tr-Complexation of thiophene in compounds of the type 123 activates the heterocycle relative toward other nucleophiles, such as OMe , SMe , SEt , S(i-Pr) , andCH(COOMe)2. The products 127 include the ring-opened butadiene-thiolate framework. [Pg.22]

Thiophene, benzo[d]thiophene and dibenzo[d,organosulfur compounds formed at Rh- and Ir-mediated thiophene ring opening 97SL643. [Pg.223]

Benzo[c]thiophene is a source of 3-substituted derivatives of 3,4-dihydro-1//-2-benzothiopyrans via ring opening to the dianion and subsequent reaction with electrophiles <96JOC1859>. [Pg.304]

The progress on S-C bond activation, which covers the reduction of a C-S bond to a C-H bond, cross coupling reaction of sulfides with main group organometaUic nucleophiles, ring opening reactions of thietanes and thiiranes, and desulfurization of thiols, sulfides, and thiophenes has already been reviewed elsewhere [6-10], and... [Pg.217]


See other pages where Thiophene opening is mentioned: [Pg.820]    [Pg.820]    [Pg.525]    [Pg.222]    [Pg.29]    [Pg.36]    [Pg.47]    [Pg.58]    [Pg.79]    [Pg.81]    [Pg.143]    [Pg.140]    [Pg.891]    [Pg.891]    [Pg.892]    [Pg.105]    [Pg.7]    [Pg.8]    [Pg.12]    [Pg.20]    [Pg.29]    [Pg.31]    [Pg.34]    [Pg.37]    [Pg.38]    [Pg.39]    [Pg.40]    [Pg.44]    [Pg.45]    [Pg.47]    [Pg.51]    [Pg.53]    [Pg.129]    [Pg.101]    [Pg.88]    [Pg.126]    [Pg.76]    [Pg.420]    [Pg.154]    [Pg.61]   
See also in sourсe #XX -- [ Pg.31 , Pg.299 ]

See also in sourсe #XX -- [ Pg.27 ]




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3- -2-thiophene Open-Chain Compound

Ring-opening metathesis thiophenes

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