Zobrazeno 1 - 10
of 11
pro vyhledávání: '"ANDREA C. BOICELLI"'
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :249-252
Chemical and spectroscopic data clearly demonstrate that all the title compounds are acetylated only at the exocyclic nitrogen.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3dc5b508805395ee96047fa4b95b432b
https://doi.org/10.1039/p19780000249
https://doi.org/10.1039/p19780000249
Publikováno v:
Journal of Heterocyclic Chemistry. 14:257-260
The 1H and 13C nmr spectra of three cyclic sulphonium salts ol dithiacyclophanes have been recorded and compared with those of the open-chain analogue. The 1H spectra indicate that methylation of the dithiacyclophanes gives a mixture of eonformationa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c62a134a46503c8880120f1c1fc92ac
https://doi.org/10.1002/jhet.5570140219
https://doi.org/10.1002/jhet.5570140219
Publikováno v:
The Journal of Organic Chemistry. 44:2087-2092
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a044a387dcfc402a6a3c445c020f39c
https://doi.org/10.1021/jo01327a009
https://doi.org/10.1021/jo01327a009
Publikováno v:
J. Chem. Soc., Perkin Trans. 2. :1396-1400
The interpretation of the 1H n.m.r. spectrum of a meta-substituted biphenyl (3,3′,5,5′-tetrachlorobiphenyl) dissolved in the nematic phase of a liquid crystalline solvent showed unambiguously that in solution it has neither a planar structure nor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4bc0b41a2f81c6d925274e97004bd52b
https://doi.org/10.1039/p29730001396
https://doi.org/10.1039/p29730001396
Publikováno v:
Synthesis. 1981:570-572
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::69da2d771d1cbcf2afa6113c878b545a
https://doi.org/10.1055/s-1981-29533
https://doi.org/10.1055/s-1981-29533
Publikováno v:
Chemischer Informationsdienst. 5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::418196070d17018a1af9595dae64e488
https://doi.org/10.1002/chin.197449111
https://doi.org/10.1002/chin.197449111
Publikováno v:
Chemischer Informationsdienst. 5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49cbfdb0d3a6223d12c15ffb2508e454
https://doi.org/10.1002/chin.197433087
https://doi.org/10.1002/chin.197433087
Publikováno v:
Tetrahedron Letters. 16:1205-1206
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::55db468f41093d72ddea4182585eb027
https://doi.org/10.1016/s0040-4039(00)72095-8
https://doi.org/10.1016/s0040-4039(00)72095-8
Publikováno v:
Tetrahedron Letters. 19:1213-1214
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4661cebd3282af9a5c4ccac182da622
https://doi.org/10.1016/s0040-4039(01)94502-2
https://doi.org/10.1016/s0040-4039(01)94502-2
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 2. :1024
The 13C n.m.r. spectra of the four symmetrical naphthyridines have been obtained and assignment of the signals performed by means of heteronuclear decoupling experiments and empirical additivity methods. The shifts were found to depend linearly upon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b6e34ae813fbb18d0cad185531301be
https://doi.org/10.1039/p29730001024
https://doi.org/10.1039/p29730001024