Zobrazeno 1 - 10
of 196
pro vyhledávání: '"Pierre Demerseman"'
Publikováno v:
Bulletin des Sociétés Chimiques Belges. 100:539-548
The retro-Fries rearrangement, catalyzed by protic and Lewis acids, was studied for some o-hydroxyketones. The results are consistent with the mechanism of an heterolytic cleavage and rearrangement. It appears that, in general, Lewis acids do not ind
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8fcf62ee69820ed6f246e261ea6e4e18
https://doi.org/10.1002/bscb.19911000709
https://doi.org/10.1002/bscb.19911000709
Publikováno v:
Journal of Heterocyclic Chemistry. 33:973-977
New functionalized α-carbolinones especially the 4-hydroxy-3-nitro-1H,9H-pyrido[2,3-b]indol-2-one were synthesized in a good yield, three-step reaction. A complete 13C, 15N nmr study of this carbolinone and precursors is presented.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40c1640f1bc69112ce48958e9f2e94c0
https://doi.org/10.1002/jhet.5570330368
https://doi.org/10.1002/jhet.5570330368
Publikováno v:
Journal of Heterocyclic Chemistry. 32:17-24
1,6-Dioxabenzo[a]pyrene, the first dioxa-analog of benzo[a]pyrene, was synthesized from 5-methoxy-1-naphthol in an eight-step reaction involving two peri-heterocyclizations.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8c9c8c8e5bf2a3a427485795ff8a223
https://doi.org/10.1002/jhet.5570320103
https://doi.org/10.1002/jhet.5570320103
Autor:
G. Lamotte, J. M. Gillardin, F. Lepage, S. Risse, Pierre Demerseman, Daniel Dauzonne, R. Pointet
Publikováno v:
European Journal of Medicinal Chemistry. 30:53-59
Summary A series of novel benzofuranylacryloylpiperazines, which are structurally related to both cinnamamide derivatives and befuraline, have been prepared as their hydrochlorides. Their anticonvulsant and antidepressant activities against seizures
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::37e05562cb59498051a036a17903a7fc
https://doi.org/10.1016/0223-5234(96)88209-2
https://doi.org/10.1016/0223-5234(96)88209-2
Autor:
J.‐P. Bideau, J. Kotzyba, M. Cotrait, J.‐P. Buisson, N. Platzer, Pierre Demerseman, J.‐P. Lievremont
Publikováno v:
Journal of Heterocyclic Chemistry. 30:739-747
1,8-Dioxapyrene, a novel unsubstituted dioxa-analog of pyrene was synthesized from 4-methoxy-1-naphthol in a ten-step reaction involving two peri-heterocyclizations- 1 H and 13 C nmr indicated a disruption of extended delocalization of π electrons,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3417f546c90f854efa2246665cf71044
https://doi.org/10.1002/jhet.5570300324
https://doi.org/10.1002/jhet.5570300324
Publikováno v:
Applied Spectroscopy. 47:317-320
Fluorescence emission spectra are reported for benzo[b]naphtho[2,3d]furan, dinaphtho[l,2b:l′,2′d]furan, dinaphtho[2,lb:l′,2′d]furan, dibenzo[2,3:10,11]perylo[l,12bcd]furan, dibenzo[2,3:10,ll]perylo-(l,12bcd]thiophene, naphtho[l,8bc:5,4b′c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::93c94f2acf76d5efb40f4b7e39575f3a
https://doi.org/10.1366/0003702934066622
https://doi.org/10.1366/0003702934066622
Publikováno v:
Acta Crystallographica Section C Crystal Structure Communications. 49:264-267
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c67f4687f1a9c37499f20443f7220f4
https://doi.org/10.1107/s0108270192006875
https://doi.org/10.1107/s0108270192006875
Autor:
Helene Strapelias, Henri Pezerat, Pierre Demerseman, Maurice Duquesne, J.-P. Buisson, Roger Zalma, Odilon Chalvet
Publikováno v:
Free Radical Research Communications. 18:229-237
Generation of radical anions during NADPH reduction of four mutagenic and genotoxic alpha-nitroarenofurans was examined. ESR showed that free radicals were generated during reduction solely in the presence of light. Computer simulations of ESR spectr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3e9f68fceac52bdf9327836ab5821e2
https://doi.org/10.3109/10715769309145872
https://doi.org/10.3109/10715769309145872
Autor:
Robert Martin, Pierre Demerseman
Publikováno v:
ChemInform. 23
The titanium(IV) chloride-mediated Fries rearrangement of 3,4-dialkylphenyl benzoates 1 yields mainly 4,5-dialkyl-2-hydroxy-benzophenones 2 in high yield. We describe here a new access to the unknown vicinal 2,3-dialkyl-6-hydroxybenzophenones 3, whic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ebd61a3f8ecdc0278b21f5284cdcdc49
https://doi.org/10.1002/chin.199250141
https://doi.org/10.1002/chin.199250141
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bccb6e9b790835952a29868260dd5992
https://doi.org/10.1002/chin.199122107
https://doi.org/10.1002/chin.199122107