Zobrazeno 1 - 10
of 38
pro vyhledávání: '"J. Beauhaire"'
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5bb6f74ee2db12f83d7411a49bc08cc6
https://doi.org/10.1002/chin.199124170
https://doi.org/10.1002/chin.199124170
Publikováno v:
Organic Preparations and Procedures International. 24:665-669
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::412f583952ffee41dc1dd02db1d4d333
https://doi.org/10.1080/00304949209356241
https://doi.org/10.1080/00304949209356241
Publikováno v:
Tetrahedron Letters
Tetrahedron Letters, Elsevier, 1990, 31 (27), pp.3883-3886. ⟨10.1016/S0040-4039(00)97495-1⟩
Tetrahedron Letters, Elsevier, 1990, 31 (27), pp.3883-3886. ⟨10.1016/S0040-4039(00)97495-1⟩
A general sytnthetic strategy for 1-hytdroxy nortropane skeleton, the common feature of calystegines, is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d2d6865c3d83caddfce6ea3aa761552
https://doi.org/10.1016/s0040-4039(00)97495-1
https://doi.org/10.1016/s0040-4039(00)97495-1
Publikováno v:
Proceedings of The 9th International Electronic Conference on Synthetic Organic Chemistry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::adc8eff08634101f5342cd395cd7dfd6
https://doi.org/10.3390/ecsoc-9-01468
https://doi.org/10.3390/ecsoc-9-01468
Publikováno v:
Tetrahedron Letters. 25:2751-2754
Absintholide 1 is a new guaianolide dimer whose structure and stereochemistry has been elucidated on the basis of high resolution n.m.r.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2270062c6fe991681054fa3cc5ae05c3
https://doi.org/10.1016/s0040-4039(01)81281-8
https://doi.org/10.1016/s0040-4039(01)81281-8
Publikováno v:
Tetrahedron Letters. 21:3191-3194
Absinthin, a constituent of A . absinthium , has been given structure 2 .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d59ba033874f1f77bf589177eee53955
https://doi.org/10.1016/s0040-4039(00)77442-9
https://doi.org/10.1016/s0040-4039(00)77442-9
Dimeric sesquiterpene lactone. Structure of isoabsinthin acid isomerization of absinthin derivatives
Publikováno v:
Tetrahedron Letters. 22:2269-2272
Isoabsinthin 2 is a new diguaianolide constituent of A.absinthium 1. The acid isomerizations of several derivatives of absinthin have been studied.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::126fa499df2acf532733b8d53466a983
https://doi.org/10.1016/s0040-4039(01)92907-7
https://doi.org/10.1016/s0040-4039(01)92907-7
Publikováno v:
ChemInform. 18
The N-phenacylarylamine (4) gives the N,N-diphenacyl derivative (5) on treatment with phenacyl bromide under phase-transfer catalysis conditions. Condensation of (5) with an arylamine results in the formation of the thermally stable 1,4-diaryl-3,5-di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::31216e5a210b828adb14a1aa34d0e4ce
https://doi.org/10.1002/chin.198748221
https://doi.org/10.1002/chin.198748221
Autor:
J. BEAUHAIRE, J.-L. FOURREY
Publikováno v:
Chemischer Informationsdienst. 13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec9a5a6c2b5a06958074b25388d3dbf3
https://doi.org/10.1002/chin.198224326
https://doi.org/10.1002/chin.198224326
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1
Journal of the Chemical Society, Perkin Transactions 1, Royal Society of Chemistry, 1987, pp.1841-1843
Journal of the Chemical Society, Perkin Transactions 1, Royal Society of Chemistry, 1987, pp.1841-1843
The N-phenacylarylamine (4) gives the N,N-diphenacyl derivative (5) on treatment with phenacyl bromide under phase-transfer catalysis conditions. Condensation of (5) with an arylamine results in the formation of the thermally stable 1,4-diaryl-3,5-di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14cceba8558f3cd3eb0a89966ba6c86f
https://hal.inrae.fr/hal-02726112
https://hal.inrae.fr/hal-02726112
