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pro vyhledávání: '"Cabon, Y.H.M."'
This paper describes a mechanistic study of the SCS-pincer PdII-catalyzed auto-tandem reaction consisting of the stannylation of cinnamyl chlo- ACHTUNGTRENUNGride with hexamethylditin, followed by an electrophilic allylic substitution of the primary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______101::1d86fa016324d1bf5c078a658608074b
https://dspace.library.uu.nl/handle/1874/290560
https://dspace.library.uu.nl/handle/1874/290560
Autor:
Pijnenburg, N.J.M., Cabon, Y.H.M., van Koten, G., Klein Gebbink, R.J.M., Organic Chemistry and Catalysis, Sub Chem Biol & Organic Chem begr 1-6-12
Publikováno v:
Chemistry-A European Journal, 19(15), 4858. Wiley
This paper describes a mechanistic study of the SCS-pincer PdII-catalyzed auto-tandem reaction consisting of the stannylation of cinnamyl chlo- ACHTUNGTRENUNGride with hexamethylditin, followed by an electrophilic allylic substitution of the primary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::debebff6fe842e932bcb1f252c1c1403
https://pubmed.ncbi.nlm.nih.gov/23436343
https://pubmed.ncbi.nlm.nih.gov/23436343
Autor:
Cabon, Y.H.M., Klein Gebbink, R.J.M., Deelman, B.J., Organic Chemistry and Catalysis, Sub Chem Biol & Organic Chem begr 1-6-12
Publikováno v:
Dalton Transactions, 40(34), 8651. Royal Society of Chemistry
[Pd(PPh(3))(4)] catalyzes the dehydrostannylation of n-alkyltin trichlorides into HSnCl(3)(THF)(n) and isomers of the corresponding alkene. The reaction mechanism involves oxidative addition of the Sn-C bond followed by β-H elimination from the resu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94decf48c0851b5ad103f2d80b8d1368
https://pubmed.ncbi.nlm.nih.gov/21804998
https://pubmed.ncbi.nlm.nih.gov/21804998