Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Futoshi Abe"'
Publikováno v:
IEEJ Transactions on Power and Energy. 121:699-707
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::86c2b3900ef88231f6cd6ab909ad24a4
https://doi.org/10.1541/ieejpes1990.121.6_699
https://doi.org/10.1541/ieejpes1990.121.6_699
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :2651-2655
Reactions of the kinetic enolates 6 of 1-acetylcyclohexenes 5 with α-bromo α,β-unsaturated esters 7 proceed via a successive Michael–Michael-substitution pathway to give methyl 2-oxotricyclo[4.4.0.01,5]decane-5-carboxylates 8 in a one-pot operat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7c23ae19e5792286eb900e4df6ed0cae
https://doi.org/10.1039/p19930002651
https://doi.org/10.1039/p19930002651
Publikováno v:
ChemInform. 23
Reactions of the kinetic enolates of 1-acetylcyclohexenes with α-bromo-α,β-unsaturated esters afford 5-methoxycarbonyltricyclo[4.4.0.01,5]decan-2-ones in one pot syntheses via successive Michael–Michael-substitution reactions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c1186562e44af9ca18c1dae6df32f2b
https://doi.org/10.1002/chin.199211075
https://doi.org/10.1002/chin.199211075
Publikováno v:
ChemInform. 25
Reactions of the kinetic enolates 6 of 1-acetylcyclohexenes 5 with α-bromo α,β-unsaturated esters 7 proceed via a successive Michael–Michael-substitution pathway to give methyl 2-oxotricyclo[4.4.0.01,5]decane-5-carboxylates 8 in a one-pot operat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36e19d4cc9278e915ebd030494b60fe8
https://doi.org/10.1002/chin.199407074
https://doi.org/10.1002/chin.199407074
Publikováno v:
Journal of the Chemical Society, Chemical Communications. :1070
Reactions of the kinetic enolates of 1-acetylcyclohexenes with α-bromo-α,β-unsaturated esters afford 5-methoxycarbonyltricyclo[4.4.0.01,5]decan-2-ones in one pot syntheses via successive Michael–Michael-substitution reactions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::baa0bb010c3a7fab47e39a316ca70af8
https://doi.org/10.1039/c39910001070
https://doi.org/10.1039/c39910001070