Harper, Kaid C’s team published research in Journal of the American Chemical Society in 2013-02-20 | 5455-94-7

Journal of the American Chemical Society published new progress about Aliphatic ketones Role: RCT (Reactant), RACT (Reactant or Reagent). 5455-94-7 belongs to class tetrahydrofurans, and the molecular formula is C8H14O2, Product Details of C8H14O2.

Harper, Kaid C.; Vilardi, Sarah C.; Sigman, Matthew S. published the artcile< Prediction of Catalyst and Substrate Performance in the Enantioselective Propargylation of Aliphatic Ketones by a Multidimensional Model of Steric Effects>, Product Details of C8H14O2, the main research area is catalyst substrate performance enantioselective propargylation aliphatic ketone steric effect.

The effectiveness of a new asym. catalytic methodol. is often weighed by the number of diverse substrates that undergo reaction with high enantioselectivity. Here we report a study that correlates substrate and ligand steric effects to enantioselectivity for the propargylation of aliphatic ketones. The math. model is shown to be highly predictive when applied to substrate/catalyst combinations outside the training set.

Journal of the American Chemical Society published new progress about Aliphatic ketones Role: RCT (Reactant), RACT (Reactant or Reagent). 5455-94-7 belongs to class tetrahydrofurans, and the molecular formula is C8H14O2, Product Details of C8H14O2.

Referemce:
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem