Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Keisuke Hirama"'
Publikováno v:
Symmetry, Vol 3, Iss 2, Pp 155-164 (2011)
Asymmetric Michael addition of carbon nucleophiles, nitroalkanes and a β-ketoester, to enones was investigated by using a primary amino acid lithium salt as a catalyst.
Externí odkaz:
https://doaj.org/article/b02ed799888a4b50a27fb85df8174a84
Autor:
Keisuke HIRAMA, Reiji HAYATA, Taichi SEKI, Daichi KOBAYASHI, Tsutomu TAKAHASHI, Tomohiko ASAI
Publikováno v:
Plasma and Fusion Research. 18:2401028-2401028
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::06423038fd8cf837bb519622914192e1
https://doi.org/10.1585/pfr.18.2401028
https://doi.org/10.1585/pfr.18.2401028
Publikováno v:
Tetrahedron Letters. 50:7297-7299
Siloxy amino acid lithium salt, O - tert -butyldiphenylsilyl l -serine lithium salt, was found to be an effective catalyst for the asymmetric Michael addition reaction of malonates to enones.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c63acd36ef1c40c89a5e85f90866c1e8
https://doi.org/10.1016/j.tetlet.2009.10.033
https://doi.org/10.1016/j.tetlet.2009.10.033
Publikováno v:
Symmetry; Volume 3; Issue 2; Pages: 155-164
Symmetry, Vol 3, Iss 2, Pp 155-164 (2011)
Symmetry, Vol 3, Iss 2, Pp 155-164 (2011)
Asymmetric Michael addition of carbon nucleophiles, nitroalkanes and a β-ketoester, to enones was investigated by using a primary amino acid lithium salt as a catalyst.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eeffd12b33d6dc8bcd1f9805ca8083d7
Publikováno v:
ChemInform. 41
Siloxy amino acid lithium salt, O - tert -butyldiphenylsilyl l -serine lithium salt, was found to be an effective catalyst for the asymmetric Michael addition reaction of malonates to enones.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::23361b7c3088362142610dd6f74ebd86
https://doi.org/10.1002/chin.201015025
https://doi.org/10.1002/chin.201015025