Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Philippine Lebada"'
Publikováno v:
European Journal of Organic Chemistry. 1999:675-678
rac-(E)-Opposita-4(15),7(11)-dien-12-al (1) was synthesized in 12 steps via the aldehyde 11 as the key compound. The spectroscopic data of rac-1 are identical with those of the corresponding natural product, previously isolated from Vetiver oil. Synt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e5c6712b93aa46d28628f3990a3be0d
https://doi.org/10.1002/(sici)1099-0690(199903)1999:3<675::aid-ejoc675>3.0.co
https://doi.org/10.1002/(sici)1099-0690(199903)1999:3<675::aid-ejoc675>3.0.co
Publikováno v:
Chirality. 9:380-385
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab8c7f1ef3f7f875b949cf99aabb96c4
https://doi.org/10.1002/(sici)1520-636x(1997)9:4<380::aid-chir11>3.0.co
https://doi.org/10.1002/(sici)1520-636x(1997)9:4<380::aid-chir11>3.0.co
Publikováno v:
Liebigs Annalen. 1995:1693-1696
By means of a convergent synthesis strategy, the title substance (Z)-7-oxa-β-santalol (4) was prepared starting with the side chain synthon 5-iodo-2-methyl-2-pentenylmethoxyethoxymethyl ether (7) and the bicyclic synthon ethyl 3-methylene-7-oxabicyc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::547ad84f944d3b1ae74cfa54bb6949ef
https://doi.org/10.1002/jlac.1995199509235
https://doi.org/10.1002/jlac.1995199509235
Publikováno v:
ChemInform. 30
rac-(E)-Opposita-4(15),7(11)-dien-12-al (1) was synthesized in 12 steps via the aldehyde 11 as the key compound. The spectroscopic data of rac-1 are identical with those of the corresponding natural product, previously isolated from Vetiver oil. Synt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e356652d2fe4913916549c159fa1149
https://doi.org/10.1002/chin.199928212
https://doi.org/10.1002/chin.199928212