Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Yuuya Yamada"'
Publikováno v:
Tetrahedron. 71:4413-4417
Intramolecular arylcyanation across a tri-substituted double bond proceeds to give a primary alkyl cyanide product through functionalization of C–CN and allylic C–H bonds and double C–C bond formation in a 1,3-manner by cooperative nickel/AlMe2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f4aae528f2a42bc0e657d48b62193ca6
https://doi.org/10.1016/j.tet.2015.03.012
https://doi.org/10.1016/j.tet.2015.03.012
Publikováno v:
Angewandte Chemie. 124:5777-5780
The alkylation of a variety of pyridones and pyrimidones with unactivated olefins in the presence of a Ni(0)—NHC—Lewis acid cocatalyst system proceeds with high linear-to-branched selectivity and moderate to high regioselectivity (towards positio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::032ec7a1a3977e5606933fe5a436529c
https://doi.org/10.1002/ange.201200922
https://doi.org/10.1002/ange.201200922
Publikováno v:
ChemInform. 46
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b5290f501dd775db79e091f5a5b1b4c
https://doi.org/10.1002/chin.201542042
https://doi.org/10.1002/chin.201542042
Publikováno v:
Chemistry Letters. 41(3):298-300
Nickel/Lewis acid cooperative catalysis derived from [Ni(cod)2], AlEt3, and N-heterocyclic carbene (NHC) effects highly regioselective hydrocarbamoylation of 1-alkenes. Variously substituted formamides and 1-alkenes can be employed to give a range of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f35c02fb6bfb8785593206f8c7956b4
http://hdl.handle.net/2433/193758
http://hdl.handle.net/2433/193758
Publikováno v:
Journal of the American Chemical Society. 132:13666-13668
Direct C-4-selective addition of pyridine across alkenes and alkynes is achieved for the first time by nickel/Lewis acid cooperative catalysis with an N-heterocyclic carbene ligand. A variety of substituents on both alkenes and pyridine are tolerated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe3f45d71aafc5b88f26efcc9466822d
https://doi.org/10.1021/ja106514b
https://doi.org/10.1021/ja106514b
Publikováno v:
ChemInform. 43
The alkylation of a variety of pyridones and pyrimidones with unactivated olefins in the presence of a Ni(0)—NHC—Lewis acid cocatalyst system proceeds with high linear-to-branched selectivity and moderate to high regioselectivity (towards positio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85baf3f48f6012f3a5099007d77918c1
https://doi.org/10.1002/chin.201244144
https://doi.org/10.1002/chin.201244144
Publikováno v:
ChemInform. 43
Nickel/Lewis acid cooperative catalysis derived from [Ni(cod)2], AlEt3, and N-heterocyclic carbene (NHC) effects highly regioselective hydrocarbamoylation of 1-alkenes. Variously substituted formam...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b054c6a7978e6572a0d53b9593d5ab34
https://doi.org/10.1002/chin.201233054
https://doi.org/10.1002/chin.201233054
Publikováno v:
ChemInform. 42
Direct C-4-selective addition of pyridine derivatives with various alkenes is achieved for the first time by a nickel/ Lewis acid cooperative catalysis with an N-heterocyclic carbene ligand.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d386d739c0be7b7aab9e03a7c8fc1351
https://doi.org/10.1002/chin.201108151
https://doi.org/10.1002/chin.201108151
Publikováno v:
Chemistry Letters; 3/5/2012, Vol. 41 Issue 3, p298-300, 3p
Publikováno v:
Tetrahedron. 40:1791-1793
Diastereomeric mixtures of 2-substituted 1-vinyclyclohexyl acetates (or benzoates) are rearranged stereoselectively to 2-substituted (E)-β-acetoxy(or benzoyloxy)ethylidenecyclohexanes by the catalysis of bis(acetonitrile)palladium(II) chloride. A me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5dc574f9faee2eff61f4f210e6f16a32
https://doi.org/10.1016/s0040-4020(01)91131-7
https://doi.org/10.1016/s0040-4020(01)91131-7