Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Derek C. Obenschain"'
Publikováno v:
Journal of the American Chemical Society. 142:16716-16722
The selective replacement of C-H bonds in complex molecules, especially natural products like terpenoids, is a highly efficient way to introduce new functionality and/or couple fragments. Here, we report the development of a new metal-free allylic am
Publikováno v:
Chemical Science. 11:1677-1682
A new selenophosphoramide-catalyzed diamination of terminal- and trans-1,2-disubstituted olefins is presented. Key to the success of this transformation was the introduction of a fluoride scavenger, trimethylsilyl trifluoromethanesulfonate (TMSOTf),
Autor:
Sarah E. Covington, Derek C. Obenschain, James T. Rague, Evan Halliday, C. Wade Downey, Danielle N. Confair
Publikováno v:
Tetrahedron Letters. 55:5213-5215
para-Methoxybenzyl methyl ether acts as an alkylating agent for thiols in the presence of trimethylsilyl trifluoromethanesulfonate and trialkylamine base in good yields (58–96%). Aryl ketones are alkylated under similar conditions, probably through
Autor:
C. Wade Downey, Sarah E. Covington, Derek C. Obenschain, Danielle N. Confair, Evan Halliday, James T. Rague
Publikováno v:
ChemInform. 46
para-Methoxybenzyl methyl ether acts as an alkylating agent for thiols in the presence of trimethylsilyl trifluoromethanesulfonate and trialkylamine base in good yields (58–96%). Aryl ketones are alkylated under similar conditions, probably through