Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Jaana Salo"'
Publikováno v:
Tetrahedron. 50:3537-3556
The Claisen rearrangement of vinyl allyl ether 3 in refluxing toluene leads to a mixture of (±)- Z -geissoschizine 5 and (±)-15-epi- E -geissoschizine 6 [= (±)-3-epi- E -geissoschizine 6′], whereas vinyl allyl ether 4, under the same reaction co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02666fe194512e87400013aba982ebbd
https://doi.org/10.1016/s0040-4020(01)87031-9
https://doi.org/10.1016/s0040-4020(01)87031-9
Publikováno v:
Tetrahedron. 50:9207-9222
Syntheses are reported for isositsirikine isomers 1 – 6 and (16S*)-and (16R*)-17-deoxy- E -isositsirikines 9 and 10 (Model compounds 1,2 for the “synthetically missing” (16R)- and (16S)- E -isositsirikines 7 and 8 , respectively). Predominant c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b18396e98740954624d1cee17b4eb6b
https://doi.org/10.1016/s0040-4020(01)85387-4
https://doi.org/10.1016/s0040-4020(01)85387-4
Publikováno v:
ChemInform. 25
The Claisen rearrangement of vinyl allyl ether 3 in refluxing toluene leads to a mixture of (±)- Z -geissoschizine 5 and (±)-15-epi- E -geissoschizine 6 [= (±)-3-epi- E -geissoschizine 6′], whereas vinyl allyl ether 4, under the same reaction co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b671cbabefb291b0a7bcc51382223fa5
https://doi.org/10.1002/chin.199431257
https://doi.org/10.1002/chin.199431257
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cc31dcf219bc07203ff6ec774db0a83d
https://doi.org/10.1002/chin.199451269
https://doi.org/10.1002/chin.199451269
Publikováno v:
Journal of Natural Products. 58:131-133
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::427a13722f19517b81d11c23545bbac6
https://doi.org/10.1021/np50115a020
https://doi.org/10.1021/np50115a020