Zobrazeno 1 - 9
of 9
pro vyhledávání: '"E. C. Gorincioi"'
Publikováno v:
Russian Journal of Coordination Chemistry. 47:488-501
The X-ray diffraction study of three compounds containing 2,3-dihydroxybenzaldehyde semicarbazone (H3L1) or 2-hydroxy-3-methoxybenzaldehyde semicarbazone (H2L2) shows the formation of one organic salt with protonated triethylamine [(C2H5)3NH][H2L1]·
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1c8d3f7e2bdbf364866ae430396e040e
https://doi.org/10.1134/s1070328421070034
https://doi.org/10.1134/s1070328421070034
Publikováno v:
Russian Chemical Bulletin. 52:502-504
The natural drimane sesquiterpenoid lactone 5,6-dehydro-7-oxoisodrimenin was synthesized from drim-8-en-7-one as well as from 7-oxoisodrimenin.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::13eddcd685bbf870a2b7c7329e93a176
https://doi.org/10.1023/a:1023404126195
https://doi.org/10.1023/a:1023404126195
Publikováno v:
ChemInform. 31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ebf9e4dcbdf9428a8bc8ce40f0fa66ec
https://doi.org/10.1002/chin.200036195
https://doi.org/10.1002/chin.200036195
Publikováno v:
Russian Chemical Bulletin. 49:546-548
A naturally occurring drimanic sesquiterpenic lactone, isodrimenin, was synthesized from drim-8-en-7-one (1). Compound1 was converted to the known 11,12-dihydroxydrim-8-en-7-one, which was oxidized with PCC to give 7-oxoisodrimenin. The thioketal of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8338c68c51d33fece3407af07fd34494
https://doi.org/10.1007/bf02494791
https://doi.org/10.1007/bf02494791
Publikováno v:
Russian Chemical Bulletin. 49:98-101
A synthetic route to 11-hydroxydrim-8(9)-en-7-one and 11,12-hydroxydrim-8(9)-en-7-one, valuable key intermediates for the preparation of naturally occurring biologically active drimanic sesquiterpenoids, starting from easily available drim-8(9)-en-7-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::215ee1475309ea406176ba2e10c74f1f
https://doi.org/10.1007/bf02499072
https://doi.org/10.1007/bf02499072
Autor:
M. N. Coltsa, Calin Deleanu, Aculina Aricu, Alexandru Ciocarlan, Carolina Edu, E. C. Gorincioi, Pavel F. Vlad
Publikováno v:
ChemInform. 38
An efficient two-step procedure for photooxidative dehydrogenation of drimane and 11-homodrimane compounds containing an 8-en-7-one structural unit into α,α′-dienones was elaborated. The method is based on the transformation of ketones into the r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a581d2864bf846746d3c28c011f4a09b
https://doi.org/10.1002/chin.200705181
https://doi.org/10.1002/chin.200705181
Publikováno v:
ChemInform. 34
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bedcff7ac14b09c29cbb8a3dfe110fca
https://doi.org/10.1002/chin.200338162
https://doi.org/10.1002/chin.200338162
Publikováno v:
ChemInform. 31
A naturally occurring drimanic sesquiterpenic lactone, isodrimenin, was synthesized from drim-8-en-7-one (1). Compound1 was converted to the known 11,12-dihydroxydrim-8-en-7-one, which was oxidized with PCC to give 7-oxoisodrimenin. The thioketal of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4ace5898e209e5b38f25cedb84ded00
https://doi.org/10.1002/chin.200043195
https://doi.org/10.1002/chin.200043195
Publikováno v:
Russian Chemical Bulletin; Dec2004, Vol. 53 Issue 12, p2700-2705, 6p