More research is needed about 1707-03-5

The potential utility of systematic synthetic strategy will be applicable to efficient generations of chemical libraries of compounds to find ‘hit’ molecules. In my other articles, you can also check out more blogs about 1707-03-5. Product Details of 1707-03-5.

New research progress on 1707-03-5 in 2021. Chemo-enzymatic cascade processes are invaluable due to their ability to rapidly construct high-value products from available feedstock chemicals in a one-pot relay manner. 1707-03-5, Name is Diphenylphosphinic acid, molecular formula is C12H11O2P, belongs to pyrrolines compound, is a common compound. In a patnet, author is Li, SJ, once mentioned the new application about 1707-03-5, Product Details of 1707-03-5.

Coupling reactions of alpha-(N-carbamoyl)alkylcuprates with enol triflates derived from cyclic beta-keto esters: A facile approach to gamma-carbamoyl-alpha,beta-enoates

alpha-(N-Carbamoylalkyl)cuprates couple with enol triflates derived from carbocyclic and heterocyclic (i.e., piperidinones) beta-keto esters. Product yields are higher with the alkyl(cyano)cuprates [i.e., RCu(CN)Li, 56-93%] than with the dialkylcuprate reagents (i.e., R2CuLi.LiCN). An enol nonaflate works as well as the corresponding enol triflate. A facile synthetic route to gamma-amino alpha,beta-enoates not readily prepared from gamma-keto-alpha,beta-enoates is thus established. The gamma-amino-alpha, beta-enoates, available via N-Boc deprotection, can be cyclized to annulated pyrrolin-2-ones.

The potential utility of systematic synthetic strategy will be applicable to efficient generations of chemical libraries of compounds to find ‘hit’ molecules. In my other articles, you can also check out more blogs about 1707-03-5. Product Details of 1707-03-5.

Reference:
Pyrroline – Wikipedia,
,1-Pyrroline | C4H7N – PubChem