Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Hiroto HORI"'
Publikováno v:
Journal of Architecture and Planning (Transactions of AIJ). 88:867-876
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6189b07f894029033245eae378ac5b27
https://doi.org/10.3130/aija.88.867
https://doi.org/10.3130/aija.88.867
Publikováno v:
Journal of Synthetic Organic Chemistry, Japan. 77:341-350
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae04a78b6f8f5573a8458064e1f36512
https://doi.org/10.5059/yukigoseikyokaishi.77.341
https://doi.org/10.5059/yukigoseikyokaishi.77.341
Publikováno v:
Organic & Biomolecular Chemistry. 17:4783-4788
An efficient synthesis of carbo- and heterocycles using C[double bond, length as m-dash]C, C[double bond, length as m-dash]O and C[double bond, length as m-dash]N bonds under cobalt catalysis is described. The substituents on olefins are key for cont
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f763e2cedc547d6d42ddd78c157d93ae
https://doi.org/10.1039/c9ob00637k
https://doi.org/10.1039/c9ob00637k
Publikováno v:
Advanced Synthesis & Catalysis. 359:1170-1176
A nickel-catalyzed hydrocyanation triggered by hydronickelation of the carbon-carbon double bonds of allenes followed by cyclopropane cleavage is described. The observed regio- and stereochemistries in the products are strongly influenced by the init
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21bb662bafd1c475bf15e626f3a6e077
https://doi.org/10.1002/adsc.201601400
https://doi.org/10.1002/adsc.201601400
Publikováno v:
ChemInform. 46
A simple method is elaborated for the regio- and stereoselective hydrocyanation of allenes (I) to trans-alkenes (III).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba59e6a44a227c80b402479a877513ba
https://doi.org/10.1002/chin.201534056
https://doi.org/10.1002/chin.201534056
Publikováno v:
Chemical communications (Cambridge, England). 51(35)
Regio- and stereoselective hydrocyanation under nickel catalysis is described. This report shows that allenyl C–C double bonds are discriminated and converted to the corresponding carbonitriles as a single product. The key functionalities for achie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0a8e96a35e26a7a4d791055211ce051
https://pubmed.ncbi.nlm.nih.gov/25828807
https://pubmed.ncbi.nlm.nih.gov/25828807
Publikováno v:
Asian Journal of Organic Chemistry. 3:41-43
A [2+2] cycloaddition reaction of allene-ynes under thermal conditions with/without a metal complex is described. A key feature of this reaction is that a 2-benzothiazolylphenyl group bearing a CC triple bonds remarkably promotes the reaction to give
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::46a4eb3ffd2c91bec931524226f5b552
https://doi.org/10.1002/ajoc.201300218
https://doi.org/10.1002/ajoc.201300218
Publikováno v:
ChemInform. 45
The carbocyanative cyclization of allene–ynes and bis-allenes under nickel catalysis is described. The key steps are the regioselective hydronickelation of allenes and subsequent cyclization via carbometalation. The former step determines the react
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4e14c32f7f03013a7eb5cbeef2b0a0bc
https://doi.org/10.1002/chin.201415121
https://doi.org/10.1002/chin.201415121
Publikováno v:
The Journal of organic chemistry. 78(21)
The carbocyanative cyclization of allene–ynes and bis-allenes under nickel catalysis is described. The key steps are the regioselective hydronickelation of allenes and subsequent cyclization via carbometalation. The former step determines the react
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5cbd43103589bbf2e6c0d1e1654964ae
https://pubmed.ncbi.nlm.nih.gov/24070550
https://pubmed.ncbi.nlm.nih.gov/24070550
Publikováno v:
Advanced Synthesis & Catalysis. 4/3/2017, Vol. 359 Issue 7, p1170-1176. 7p.