Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Sana Ito"'
Publikováno v:
ChemInform. 41
The process provides a new and efficient approach to fluorenone imine derivatives and the nature of the isocyanide has a strong influence on the success.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d121aec28a1979a356a2c770b16ec50
https://doi.org/10.1002/chin.201049082
https://doi.org/10.1002/chin.201049082
Publikováno v:
The Journal of organic chemistry. 75(14)
To demonstrate the utility of isocyanides in catalytic C-H bond functionalization reactions, a palladium-catalyzed cyclocoupling reaction of 2-halobiaryls with isocyanides was developed. The reaction afforded an array of fluorenone imine derivatives
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ace55afc825055d4a11a17fbdad0ade2
https://pubmed.ncbi.nlm.nih.gov/20550203
https://pubmed.ncbi.nlm.nih.gov/20550203
Publikováno v:
ChemInform. 40
The insertion reaction of isocyanide into a C−S bond of dithioacetals is catalyzed by GaCl3 or TiCl4 to afford thioimidates containing an α-alkylthio group. Balanced thiophilicity of these Lewis acids is critical for efficient catalysis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f2a0fd9104124a0d7f07474fba79de6
https://doi.org/10.1002/chin.200915084
https://doi.org/10.1002/chin.200915084
Publikováno v:
Organic letters. 10(22)
The insertion reaction of isocyanide into a C-S bond of dithioacetals is catalyzed by GaCl3 or TiCl4 to afford thioimidates containing an alpha-alkylthio group. Balanced thiophilicity of these Lewis acids is critical for efficient catalysis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08aafd0cf2301c958ff514c34e5e45d8
https://pubmed.ncbi.nlm.nih.gov/18950189
https://pubmed.ncbi.nlm.nih.gov/18950189