Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Kierra M. M. Huihui"'
Publikováno v:
Organic Letters
Conjugate addition of organometallic reagents to enones to form silyl enol ether products is a versatile method to difunctionalize activated olefins, but the organometallic reagents required can be limiting. The reductive cross-electrophile coupling
Autor:
Lukiana L. Anka-Lufford, Laura K. G. Ackerman, Kierra M. M. Huihui, Daniel J. Weix, Nicholas J. Gower
Publikováno v:
Chemistry - A European Journal. 22:11564-11567
Cross-electrophile coupling of aryl halides with alkyl halides has thus far been primarily conducted with stoichiometric metallic reductants in amide solvents. This report demonstrates that the use of tetrakis(dimethylamino)ethylene (TDAE) as an orga
Autor:
Kierra M. M. Huihui, Laura K. G. Ackerman, Lukiana L. Anka-Lufford, Daniel J. Weix, Nicholas J. Gower
Publikováno v:
ChemInform. 47
A high-yielding cross-electrophile coupling of aryl or hetaryl halides with functionalized alkyl halides is examined.
Autor:
Jill A. Caputo, Laura K. G. Ackerman, S. Kim, Astrid M. Olivares, Amanda M. Spiewak, Kierra M. M. Huihui, Daniel J. Weix, Zulema Melchor, Keywan A. Johnson, Tarah A. DiBenedetto
Publikováno v:
ChemInform. 47
A new method for the decarboxylative coupling of alkyl N-hydroxyphthalimide esters (NHP esters) with aryl iodides is presented. In contrast to previous studies that form alkyl radicals from carboxylic acid derivatives, no photocatalyst, light, or ary