Trichlormethine

Application Mild Lewis acid used for stereoselective aldol and Michael reactions [2,3]-Wittig and Ireland-Claisen rearrangements Horner-Wadsworth-Emmons reactions asymmetric [3 + 2] cycloaddition ring opening reactions and Friedel-Crafts

Tin(IV) bis(acetylacetonate) dichloride

Tri(ethylene glycol) bis(chloroformate)

Triacetoxy(methyl)silane

Tributyl borate is an organoboron compound, that is often used as a reagent in organic synthesis for the preparation of various boronic acid derivatives, which are widely used in Suzuki coupling reactions in the synthesis of biaryls and other

Tributyl borate is an organoboron compound, that is often used as a reagent in organic synthesis for the preparation of various boronic acid derivatives, which are widely used in Suzuki coupling reactions in the synthesis of biaryls and other

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Green Chemistry. This product is environmentally-benign and can replace highly toxic phthalates in membrane preparation and thus

Tributyltin chloride is a salt derivative of tributyltin which is an organotin compound. Application Refer to the product&#8242s Certificate of Analysis for more information on a suitable instrument technique.

This vinylstannane undergoes Stille coupling with a vinyl triflate, giving, after hydrolysis, an &#945,&#946 &#8722unsaturated ketone, thus acting as an acetyl anion equivalent. Application Electrophilic methyl ketone equivalent used in a recent

This vinylstannane undergoes Stille coupling with a vinyl triflate, giving, after hydrolysis, an &#945,&#946 &#8722unsaturated ketone, thus acting as an acetyl anion equivalent. Application Electrophilic methyl ketone equivalent used in a recent

This vinylstannane undergoes Stille coupling with a vinyl triflate, giving, after hydrolysis, an &#945,&#946 &#8722unsaturated ketone, thus acting as an acetyl anion equivalent. Application Electrophilic methyl ketone equivalent used in a recent

This vinylstannane undergoes Stille coupling with a vinyl triflate, giving, after hydrolysis, an &#945,&#946 &#8722unsaturated ketone, thus acting as an acetyl anion equivalent. Application Electrophilic methyl ketone equivalent used in a recent