Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Emre Y. Yazıcıoğlu"'
Autor:
Cihangir Tanyeli, Emre Y. Yazıcıoğlu
Publikováno v:
Tetrahedron: Asymmetry. 23:1694-1699
A one step Pd-catalyzed coupling methodology involving a reaction between a chiral diamine and a 2-bromo-4-(alkylamino)pyridine, was developed for the synthesis of novel C2-symmmetrical chiral compounds with chemical yields of up to 87%. The organoca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16020dbfd683ab838fd2280ba6d3133b
https://doi.org/10.1016/j.tetasy.2012.11.007
https://doi.org/10.1016/j.tetasy.2012.11.007
Publikováno v:
Helvetica Chimica Acta. 91:1148-1155
Alkylbenzenes are synthesized for the first time from aliphatic hydrocarbons via an one pot, transition metal-free coupling approach under basic conditions. The method consists of two steps: condensation of 2-bromoprop-2-enyl- or 2-propargylcyclohexa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0216147a87de594e2935befdb960c09b
https://doi.org/10.1002/hlca.200890124
https://doi.org/10.1002/hlca.200890124
Publikováno v:
ChemInform. 39
Alkylbenzenes are synthesized for the first time from aliphatic hydrocarbons via an one pot, transition metal-free coupling approach under basic conditions. The method consists of two steps: condensation of 2-bromoprop-2-enyl- or 2-propargylcyclohexa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b7dc89ce1cb07234334ed006d283e26c
https://doi.org/10.1002/chin.200842053
https://doi.org/10.1002/chin.200842053
Publikováno v:
ChemInform. 36
We describe the preliminary results of one-pot syntheses of various N-substituted 2-methyl-4,5,6,7-tetrahydroindole derivatives from 2-(2-bromoallyl)cyclohexanone and the corresponding primary amines in good yields. Aliphatic amines were directly con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2666dbed0c554c07790779f4543ace8
https://doi.org/10.1002/chin.200515109
https://doi.org/10.1002/chin.200515109