Zobrazeno 1 - 10
of 13
pro vyhledávání: '"J. D. Street"'
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91cb0f491705b406076914dd9f5a85ca
https://doi.org/10.1002/chin.199107241
https://doi.org/10.1002/chin.199107241
Publikováno v:
Acta Crystallographica Section C Crystal Structure Communications. 47:1523-1525
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::385cb35d068ea43eb8fb33925fa0425e
https://doi.org/10.1107/s0108270190013907
https://doi.org/10.1107/s0108270190013907
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :3193
6,7-Methoxy-1-methylisoquinoline 3a was nitrated at C-8, oxidised to the nitro aldehyde 3r and then condensed with nitromethane using alumina as base to give the alcohol 3s, dehydration of which produced the nitroethene 3t. Iron-acetic acid treatment
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ba0d2a46e9d7012b065de062cc5b144
https://doi.org/10.1039/p19900003193
https://doi.org/10.1039/p19900003193
Autor:
Frank Heatley, Martin Harris, John A. Joule, Owen S. Mills, David I. Bishop, J. D. Street, Roy L. Beddoes
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :1599-1606
Hexahydroazocino[4,3-b]indoles (2a-c) have been synthesised from 1-phenylsulphonylindole by introducing the appropriate side chain at C-2, via lithiation, and then intramolecular Mannich cyclisation. From (2c), 1,2,3,4-tetrahydro-2-phenoxycarbonyl-7-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ee5a1f5c10cc9e6ecdb4508afe7a931
https://doi.org/10.1039/p19870001599
https://doi.org/10.1039/p19870001599
Publikováno v:
Tetrahedron. 43:1903-1920
The synthesis of 2,3,5,6-tetrahydro-1H,4H,11cH-3a,6a,11b-triazabenz [de]anthracene (5) is described. X-ray crystal structure deteminations on hexahydro-1H,4H,7H,9bH-3a,6a,9a-triazaphenalene (1) and its benzoanalogue (5) show them to adopt differing c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac819273ad7054ba114c0e734ec7418e
https://doi.org/10.1016/s0040-4020(01)81503-9
https://doi.org/10.1016/s0040-4020(01)81503-9
Publikováno v:
ChemInform. 19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99af5f861fadeb72474eded5ca9ab650
https://doi.org/10.1002/chin.198844184
https://doi.org/10.1002/chin.198844184
Publikováno v:
ChemInform. 19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b6d5715c96c3e86366e8abf85a36b908
https://doi.org/10.1002/chin.198808162
https://doi.org/10.1002/chin.198808162
Publikováno v:
Chemischer Informationsdienst. 17
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a405f42842cce116c166f44db76e5e46
https://doi.org/10.1002/chin.198638053
https://doi.org/10.1002/chin.198638053
Autor:
Roy L. Beddoes, Frank Heatley, J. D. Street, D. I. Bishop, Martin Harris, O. S. Mills, J. A. Joule
Publikováno v:
ChemInform. 18
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e478c172b987b6cdd423fb9dffaa843e
https://doi.org/10.1002/chin.198744238
https://doi.org/10.1002/chin.198744238
Publikováno v:
ChemInform. 18
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::71d0d645caa504aa8405c9fe93ff903b
https://doi.org/10.1002/chin.198737240
https://doi.org/10.1002/chin.198737240