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2- Methyl-27/-naphtho thiophene

Naphtho[2,3-h]thiophene, S-methyl-theoretical methods, 4, 3 Naphtho[2,3-c]thiophene, 1,3-diphenyl-synthesis, 4, 904... [Pg.706]

Naphtho[ 1,2-h]thiophene-2-carboxylic acid synthesis, 4, 893 Naphthothiophenes synthesis, 4, 881, 907, 914 Naphthothiophenes, dihydrosynthesis, 4, 113 Naphtho[ 1,2-c]thiophenes synthesis, 4, 891 Naphtho[2, l-h]thiophenes synthesis, 4, 907 Naphtho[2,3-h]thiophenes synthesis, 4, 905, 908-909 Naphtho[ 1,8-de][l,2,3]triazine, 2-methyl-reactions... [Pg.706]

Watanabe, K. Noda, K., and Maruhashi, K., Selective cleavage of 10-methyl benzo b naphtho 2,1-d thiophene by recombinant Mycobacterium sp strain. Biotechnology, Letters, 2003. 25(10) pp. 797-803. [Pg.216]

Fig. 29. Correlation between relative hydrogenolysis reactivity and the electron densities on sulfur. ( ) Reaction conditions 300°C, 71 atm, sulfided CoO-Mo03/A1203 (5). (1) DBT (2) benzo[fo]naphtho[2,3-4]thiophene (3) 7,8,9,10-tetrahydrobenzo[b]naphtho[2,3-rf]thio-phene (4) 5b,6,ll,lla-tetrahydrobenzo[fc]naphtho[2,3-d]thiophene. (O) Reaction conditions 450°C, 1 atm, sulfided CoO-Mo03/A1203(6). (5) Thiophene (6) tetrahydrothiophene (7) benzothiophene (8) 2,3-dihydrobenzothiophene. ( + ) Reaction conditions 360°C, 2.9 MPa, sulfided NiO-Mo03/Al203(3). (9) 1-Methyl-DBT (10) 2- or 3-methyl-DBT (11) 4-methyl-DBT (12) 4,6-dimethyl-DBT. (A) Reaction conditions 300°C, 102 atm, sulfided CoO-Mo03/ Al203(8). (13) 2,8-Dimethyl-DBT (14) 3,7-dimethyl-DBT (15) 4-methyl-DBT (16) 4,6-di-methyl-DBT. Reprinted with permission from Ref. 38, Ma et al. (1995). Copyright 1995 American Chemical Society. Fig. 29. Correlation between relative hydrogenolysis reactivity and the electron densities on sulfur. ( ) Reaction conditions 300°C, 71 atm, sulfided CoO-Mo03/A1203 (5). (1) DBT (2) benzo[fo]naphtho[2,3-4]thiophene (3) 7,8,9,10-tetrahydrobenzo[b]naphtho[2,3-rf]thio-phene (4) 5b,6,ll,lla-tetrahydrobenzo[fc]naphtho[2,3-d]thiophene. (O) Reaction conditions 450°C, 1 atm, sulfided CoO-Mo03/A1203(6). (5) Thiophene (6) tetrahydrothiophene (7) benzothiophene (8) 2,3-dihydrobenzothiophene. ( + ) Reaction conditions 360°C, 2.9 MPa, sulfided NiO-Mo03/Al203(3). (9) 1-Methyl-DBT (10) 2- or 3-methyl-DBT (11) 4-methyl-DBT (12) 4,6-dimethyl-DBT. (A) Reaction conditions 300°C, 102 atm, sulfided CoO-Mo03/ Al203(8). (13) 2,8-Dimethyl-DBT (14) 3,7-dimethyl-DBT (15) 4-methyl-DBT (16) 4,6-di-methyl-DBT. Reprinted with permission from Ref. 38, Ma et al. (1995). Copyright 1995 American Chemical Society.
Photoirradiation of 158e in the presence of iodine affords the benzo[6]naphtho[2,l-d]thiophene (159) 158a-d similarly give the appropriate methyl-substituted compounds.465 With ethyl diazo-... [Pg.261]

The formation of naphtho[6c]thiophene-3-ones 106 takes place on acylation of 2-substituted benzo[b]thiophenes 103 with cinnamoyl chloride (78AP710, 78LA627 79LA965). Interestingly, the aromatization of the intermediate 105 occurs with elimination of benzene. Chalcone 104 also may be obtained on acetylation of benzo[fe]thiophene 103, followed by condensation of benzaldehyde with the methyl group of the 3-acetylbenzo[b]thiophene intermediate (79LA965). [Pg.20]

Cava and Pollack s elegant synthesis of benzo[c]thiophene52 has been extended to the synthesis of, for example, naphtho[l,2-c]thio-phene (47),52 methyl benzo[c]thiophene-5-carboxylate,54 and 1,3-dimethyl- (48)55 and l,3,4,6-tetraphenylthieno[3,4-c]thiophene (49).56 The last compound is of particular interest because it is a remarkably stable (cf. compound 48 which only exists transiently) nonclassical thiophene containing ten n electrons for which the only uncharged resonance structure (49) contains a tetravalent sulfur atom. When the sulfoxide (50) is pyrolyzed over aluminum oxide, it gives the parent cyclic sulfide and 51 by disproportionation.57 However, when 50 is heated in acetic anhydride in the presence of iV-phenylmaleimide,... [Pg.351]


See other pages where 2- Methyl-27/-naphtho thiophene is mentioned: [Pg.42]    [Pg.254]    [Pg.278]    [Pg.59]    [Pg.909]    [Pg.909]    [Pg.414]    [Pg.1112]    [Pg.186]    [Pg.791]    [Pg.48]    [Pg.37]    [Pg.45]   
See also in sourсe #XX -- [ Pg.17 , Pg.51 ]




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