Trichlormethine

Application Refer to the product&#8242s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Application Use of TIPS substituted alkynes in a preparation of silyl vinyl ketenes from chromium carbene complexes.

Application Use of TIPS substituted alkynes in a preparation of silyl vinyl ketenes from chromium carbene complexes.

Application Use of TIPS substituted alkynes in a preparation of silyl vinyl ketenes from chromium carbene complexes.

Application Used to prepare silyloxy acetylenes from lithium acetylides the silyloxy acetylenes were then employed in protic acid-promoted cyclizations of arenes, alkynes and olefins.

Application Used to prepare silyloxy acetylenes from lithium acetylides the silyloxy acetylenes were then employed in protic acid-promoted cyclizations of arenes, alkynes and olefins.

Trimethyl(tributylstannyl)silane

Application Trimethyl(trifluoromethyl)silane can be used as a trifluoromethylating agent in the following processes: Conversion of N -( tert -butylsulfinyl)-imines to trifluoromethylated amines Conversion of trans -enones to trans

Application Trimethyl(trifluoromethyl)silane can be used as a trifluoromethylating agent in the following processes: Conversion of N -( tert -butylsulfinyl)-imines to trifluoromethylated amines Conversion of trans -enones to trans

Trimethyl(trifluoromethyl)silane (TMSCF 3 ) is also called as Ruppert-Prakash fluorination reagent. It is extensively used for the synthesis of trifluoromethyl-containing compounds.

Trimethyl(trifluoromethyl)silane (TMSCF 3 ) is also called as Ruppert-Prakash fluorination reagent. It is extensively used for the synthesis of trifluoromethyl-containing compounds.

Application Trimethylsilyl trifluoromethanesulfonate has been used in combination with boron trifluoride etherate for the copper-catalyzed asymmetric allylic alkylation (AAA) of allyl bromides, chlorides, and ethers with organolithium reagents in