Zobrazeno 1 - 10
of 106
pro vyhledávání: '"R. C. Cookson"'
Publikováno v:
Organic Syntheses
4-Phenyl-1,2,4-triazoline-3,5-dione intermediate: 52 g. (0.50 mole) of ethyl hydrazinecarboxylate in 550 ml. of dry benzene intermediate: 4-phenyl-1-carbethoxysemicarbazide intermediate: 4-phenylurazole product: 4-(4-nitrophenyl)urazole product: 4-te
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5fad501dbbc31729acd691ad35fc2694
https://doi.org/10.1002/0471264180.os051.30
https://doi.org/10.1002/0471264180.os051.30
Autor:
R. C. Cookson, R. R. Hill
Publikováno v:
J. Chem. Soc.. :2023-2026
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::48f33c83503173758b2e2e877481abad
https://doi.org/10.1039/jr9630002023
https://doi.org/10.1039/jr9630002023
Publikováno v:
J. Chem. Soc.. :1563-1567
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0da176958ab07b2413fa36b069e2bf64
https://doi.org/10.1039/jr9640001563
https://doi.org/10.1039/jr9640001563
Publikováno v:
J. Chem. Soc.. :1224-1228
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::deb826d358734abc63cfcce4a1e29108
https://doi.org/10.1039/jr9610001224
https://doi.org/10.1039/jr9610001224
Autor:
J. Hudec, R. C. Cookson
Publikováno v:
J. Chem. Soc.. :429-434
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::259fcc504d8e5c62f7d3bdf7318e730a
https://doi.org/10.1039/jr9620000429
https://doi.org/10.1039/jr9620000429
Autor:
M. J. Nye, R. C. Cookson
Publikováno v:
J. Chem. Soc.. :2009-2018
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d32fa7ac848ff0015e61f80e2d2414b
https://doi.org/10.1039/jr9650002009
https://doi.org/10.1039/jr9650002009
Publikováno v:
J. Chem. Soc. B. :215-226
The ultraviolet spectra and circular dichroism of dehydrocamphor and dehydroepicamphor show the effects of mixing the n→π* and π→π* transitions, which reach an extreme in their aryl derivatives. The 3-arylborn-2-en-6-ones have [α]D of about 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff326751827b534543245c0c6245b534
https://doi.org/10.1039/j29670000215
https://doi.org/10.1039/j29670000215
Publikováno v:
J. Chem. Soc. C. :1905-1909
The title compound has been shown to be a powerful dienophile with a wide variety of dienes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::87ecb22a8caa1c7c8fe5e1450ecbca50
https://doi.org/10.1039/j39670001905
https://doi.org/10.1039/j39670001905
Publikováno v:
J. Chem. Soc. C. :2494-2500
U.v. irradiation of 3β-acetoxy-5α-hydroxycholestan-6-one (I; R = Ac) and of the 5β-epimer (VI; R = Ac) through Pyrex gives 3β-acetoxy-5α-hydroxy-5,6-secocholestan-6-oic lactone (II; R = Ac) and its 5β-epimer respectively, in almost quantitative
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::498f6274a03bf7ed78d012456e95a36b
https://doi.org/10.1039/j39680002494
https://doi.org/10.1039/j39680002494
Publikováno v:
J. Chem. Soc.. :5041-5050
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::19363671cb0a638811057bab4d1159da
https://doi.org/10.1039/jr9570005041
https://doi.org/10.1039/jr9570005041