Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Taketoshi Ohkubo"'
Publikováno v:
Tetrahedron Letters. 37:7075-7078
Enantioselective synthesis of the unnatural antipode of cordiaquinone B possesing a 3-substituted 2,3,4-trimethylcyclohexanone framework was accomplished starting with (4 S , 5 S )-4-methyl-5-trimethylsilyl-2-cyclohexen-1-one. By this synthesis, the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aef1e7c7d0be2589ed20321fa07e9ff5
https://doi.org/10.1016/0040-4039(96)01556-0
https://doi.org/10.1016/0040-4039(96)01556-0
Publikováno v:
Tetrahedron Letters. 36:3365-3368
The first asymmetric total synthesis of the title compounds, unnatural enantiomers, has been achieved.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b04cde357313ddbd0d4236f68f8e7e57
https://doi.org/10.1016/0040-4039(95)00542-k
https://doi.org/10.1016/0040-4039(95)00542-k
Publikováno v:
ChemInform. 26
The first asymmetric total synthesis of the title compounds, unnatural enantiomers, has been achieved.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::edb6fbf3c442b20ab24e7d21651b54fa
https://doi.org/10.1002/chin.199535233
https://doi.org/10.1002/chin.199535233
Publikováno v:
ChemInform. 26
Enantioselective synthesis of the titled ambrosanolides is described. Use of the trimethylsilyl group as an anchor contributed to the stereoselective introduction of two methyl groups.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::298912e4b2028e423e6b6dafd9bc8dbc
https://doi.org/10.1002/chin.199533204
https://doi.org/10.1002/chin.199533204
Publikováno v:
ChemInform. 28
Enantioselective synthesis of the unnatural antipode of cordiaquinone B possesing a 3-substituted 2,3,4-trimethylcyclohexanone framework was accomplished starting with (4 S , 5 S )-4-methyl-5-trimethylsilyl-2-cyclohexen-1-one. By this synthesis, the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bdca16e60d5f6292bc20eae8c66e131b
https://doi.org/10.1002/chin.199701255
https://doi.org/10.1002/chin.199701255