“…In contrast, the direct conversion of widely available terminal alkynes to propargyl silanes is a conceptually simple and attractive approach (Scheme 1B, eqn (6)). [15][16][17][18] This strategy is usually performed by deprotonation of terminal alkynes and then a reaction with a silylmethyl electrophile, such as trimethylsilylmethyl iodide.…”
Herein we report a mild synthesis of propargyl silanes from terminal alkynes. We exploit a bromonaphthyl-substituted silane as a silylmethyl electrophile surrogate, which participates in a Sonogashira reaction after an...
“…In contrast, the direct conversion of widely available terminal alkynes to propargyl silanes is a conceptually simple and attractive approach (Scheme 1B, eqn (6)). [15][16][17][18] This strategy is usually performed by deprotonation of terminal alkynes and then a reaction with a silylmethyl electrophile, such as trimethylsilylmethyl iodide.…”
Herein we report a mild synthesis of propargyl silanes from terminal alkynes. We exploit a bromonaphthyl-substituted silane as a silylmethyl electrophile surrogate, which participates in a Sonogashira reaction after an...
Die Lithiumacetylide (I) reagieren mit den Trimethylsilylverbindungen (II) definiert zu den TrimethylsilylQ‐alkinen (III); es werden nur geringe Mengen der Isomeren (IV) und des Homologen (V) gebildet.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.