The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: 1,3,5,7-Tetramethyl-6-phenyl-2,4,8-trioxa-6-phosphaadamantane( cas:97739-46-3 ) is researched.Recommanded Product: 97739-46-3.Adjabeng, George; Brenstrum, Tim; Frampton, Christopher S.; Robertson, Al J.; Hillhouse, John; McNulty, James; Capretta, Alfredo published the article 《Palladium complexes of 1,3,5,7-tetramethyl-2,4,8-trioxa-6-phenyl-6-phosphaadamantane: Synthesis, crystal structure and use in the Suzuki and Sonogashira reactions and the α-arylation of ketones》 about this compound( cas:97739-46-3 ) in Journal of Organic Chemistry. Keywords: arylboronic acid aryl halide Suzuki coupling trioxaphosphaadamantane palladium; biaryl preparation; alkyne aryl halide Sonogashira coupling trioxaphosphaadamantane palladium; arylalkyne preparation; ketone aryl halide arylation trioxaphosphaadamantane palladium; aryl ketone preparation; trioxaphosphaadamantane palladium coupling catalyst. Let’s learn more about this compound (cas:97739-46-3).
Palladium complexes of 1,3,5,7-tetramethyl-2,4,8-trioxa-6-phenyl-6-phosphaadamantane were prepared and characterized with Pd[1,3,5,7-tetramethyl-2,4,8-trioxa-6-phenyl-6-phosphaadamantane]2·dba shown to be an effective catalyst for use in the Suzuki and Sonogashira reactions and the α-arylation of ketones. Couplings using this versatile complex proceeded in excellent yields under mild conditions.
Although many compounds look similar to this compound(97739-46-3)Recommanded Product: 97739-46-3, numerous studies have shown that this compound(SMILES:CC1(C2)OC(C3)(C)OC2(C)OC3(C)P1C4=CC=CC=C4), has unique advantages. If you want to know more about similar compounds, you can read my other articles.
Reference:
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics