An article Synthesis of Phosphonomethyl Tetrahydrofurans via the Mori- Tamaru Reaction of Phosphonodienes WOS:000535292300019 published article about NICKEL-CATALYZED HOMOALLYLATION; STEREOSELECTIVE-SYNTHESIS; C-NUCLEOSIDES; ANALOGS; ROUTE; DERIVATIVES; 1,3-DIENE; ALDEHYDES; PHOSPHONATE; CYCLIZATION in [Paudel, Rishi R.; Ridenour, Jeremy N.; Rath, Nigam P.; Spilling, Christopher D.] Univ Missouri, Dept Chem & Biochem, St Louis, MO 63121 USA in 2020.0, Cited 54.0. Recommanded Product: 4-Nitrobenzoic acid. The Name is 4-Nitrobenzoic acid. Through research, I have a further understanding and discovery of 62-23-7
Nickel-catalyzed reductive addition of phosphono-dienes to aldehydes (the Mori-Tamaru reaction) gives hydroxyvinyl phosphonates in good yields with excellent control of the relative stereochemistry. Base-induced cyclization of the vinyl phosphonates yields phosphonomethyl-substituted tetrahydrofurans. Inversion of the hydroxyl stereochemistry by Mitsunobu reaction and then cyclization yields a different set of phosphonomethyl-substituted tetrahydrofuran diastereoisomers.
Recommanded Product: 4-Nitrobenzoic acid. About 4-Nitrobenzoic acid, If you have any questions, you can contact Paudel, RR; Ridenour, JN; Rath, NP; Spilling, CD or concate me.
Reference:
Phthalazine – Wikipedia,
,Phthalazine | C8H6N2 – PubChem