Application
On the Way Towards Greener Transition-Metal-Catalyzed Processes as Quantified by E Factors
Second generation amphiphile which forms micelles upon dissolution in water allowing a variety of cross-coupling reactions to take place in water instead of organic solvent.Included among the possible reactions are: Olefin metathesis Pd-catalyzed cross coupling reactions including Heck, Suzuki-Miyaura, Sonogashira and Buchwald-Hartwig reactions C-H activation reactionsSecond generation amphiphile for cross-coupling reactions in water
Nonionic amphile used to increase aqueous solubility of lipophilic catalysts and substrates. Olefin metathesis, Sonogashira, Suzuki-Miyaura, and Buchwald cross-coupling reactions have been successfully performed in aqueous media employing TPGS-750-M.
General description
Learn More at the Professor and Product Portal of Professor Bruce Lipshutz.
We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product TPGS-750-M is a lead surfactant for many transition metal-catalyzed cross-couplings and has been enhanced for catalytic efficiency. Find details here.
Other Notes
Watch Professor Lipshutz talk about TPGS-750-M in this webinar:From milligrams to kilograms: synthetic chemistry following nature′s lead
Packaging
10, 50, 100 mL in glass bottle
This product has met the following criteria to qualify for the following awards: