Awesome and Easy Science Experiments about 6296-53-3

Synthetic Route of 6296-53-3, Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 6296-53-3.

Synthetic Route of 6296-53-3, Catalysts allow a reaction to proceed via a pathway that has a lower activation energy than the uncatalyzed reaction. 6296-53-3, Name is N-(1,3-Dioxo-1,3-dihydroisobenzofuran-4-yl)acetamide, SMILES is CC(NC1=CC=CC(C(O2)=O)=C1C2=O)=O, belongs to benzofurans compound. In a article, author is Zhang, Youchi, introduce new discover of the category.

Synthesis of Polysubstituted 2H-Pyran-2-ones or Phenols via One-Pot Reaction of (E)-beta-Chlorovinyl Ketones and Electron-Withdrawing Group Substituted Acetates or beta-Diketones

This paper describes a facile one-pot synthesis of highly functionalized 2H-pyran-2-ones and phenols through a base-promoted annulation of readily available beta-chlorovinyl ketones with various active methylene compounds. Conjugate addition of electron-withdrawing group substituted acetates to allenone intermediates and direct conjugate addition of beta-diketones to beta-chlorovinyl ketones reveal versatile electrophilic pathways of beta-chlorovinyl ketones under different reaction conditions. In particular, cyclocondensation is regiospecific for 3,5-disubstituted phenols. Moreover, the utility of [3+3] cyclocondensation is further illustrated by the concise synthesis of benzofuran derivative and penta- or hexa-substituted phenol construction.

Synthetic Route of 6296-53-3, Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 6296-53-3.

Reference:
Benzofuran – Wikipedia,
,Benzofuran | C8H6O – PubChem