Zobrazeno 1 - 9
of 9
pro vyhledávání: '"John N. Louris"'
Publikováno v:
Journal of Heterocyclic Chemistry. 27:1721-1725
Thieno[3,2-b]pyridine 1,1-dioxide (2) undergoes Diels-Alder condensation with the dienophiles cyclopentadiene, anthracene, and naphthacene in a manner analogous to its isomer thieno[2,3-b]pyridine 1,1-dioxide (1). Compound 2 dimerizes in refluxing xy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e601d2b62b14f80f6769fcc57968c785
https://doi.org/10.1002/jhet.5570270638
https://doi.org/10.1002/jhet.5570270638
Autor:
LeRoy H. Klemm, John N. Louris
Publikováno v:
Heterocyclic Communications. 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::01569e5695f9eac22daf0d1678ccbdbe
https://doi.org/10.1515/hc.1996.2.6.493
https://doi.org/10.1515/hc.1996.2.6.493
Autor:
LeRoy H. Klemm, John N. Louris
Publikováno v:
Heterocyclic Communications. 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::53e767d77f09fa125d5d36b68b48dd55
https://doi.org/10.1515/hc.1995.1.5-6.375
https://doi.org/10.1515/hc.1995.1.5-6.375
Publikováno v:
Journal of Chromatography A. 259:453-458
Relative retention data are reported for biphenyl, naphthalene, seven fluorine substituted biphenyls (bearing 1, 2, 8, and 10 fluorine atoms per molecule), and mono- and octafluoronaphthalenes in gas chromatography with (a) silicone fluid DC 710, (b)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0804daae2c36e228ff84789e904ade95
https://doi.org/10.1016/s0021-9673(01)88033-x
https://doi.org/10.1016/s0021-9673(01)88033-x
Publikováno v:
Journal of Heterocyclic Chemistry. 22:1249-1252
Thieno[3,2-b]pyridine (1) is oxidized to N-oxide 1a by means of m-chloroperoxybenzoic acid (83%). Compound 1a forms adducts with hydrogen chloride and picric acid and gives ring substitution alpha or gamma to the heteronitrogen atom. Thus, 1a plus ni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::791030926f274f3f03d97b9725897163
https://doi.org/10.1002/jhet.5570220522
https://doi.org/10.1002/jhet.5570220522
Publikováno v:
The Journal of Organic Chemistry. 48:1451-1454
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f6f4394b673f90ba5168bac7b37cbb6
https://doi.org/10.1021/jo00157a013
https://doi.org/10.1021/jo00157a013
Publikováno v:
Journal of Heterocyclic Chemistry. 21:1135-1140
Treatment of the N-oxide 1a of thieno[2,3-b]pyridine (1) with either (a) acetic anhydride and ethyl cyanoacetate or (b) benzoyl chloride and an enamine of cyclohexanone (Hamana reactions) serves to introduce a C-substituent at the 4-position of 1. In
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::da4c1e72bb018bf63503b4cd5d7c7668
https://doi.org/10.1002/jhet.5570210441
https://doi.org/10.1002/jhet.5570210441
Autor:
John N. Louris, LeRoy H. Klemm
Publikováno v:
Journal of Heterocyclic Chemistry. 21:785-789
Thieno[3,2-b]pyridine (1) is synthesized in 65% overall yield for two steps which consist of addition of toluene-α-thiol to 2-ethynylpyridine plus vacuum pyrolysis of the addend (7). Cis and trans forms of 7 are described. Compound 1 undergoes (a) e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b9c6875da31c0c49bab3e67bd504b44
https://doi.org/10.1002/jhet.5570210330
https://doi.org/10.1002/jhet.5570210330
Publikováno v:
Journal of Heterocyclic Chemistry. 18:1383-1387
Electron-impact mass spectra are presented for various substituted thieno[2,3-b]- and thieno[3,2-b]-pyridines. In particular, it is shown that chemical structures of alkylthienopyridines can be correlated (a) with their mass spectral fragmentation pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ffc97d913b1a410918316203af72ed7
https://doi.org/10.1002/jhet.5570180721
https://doi.org/10.1002/jhet.5570180721