Why do aromatic interactions matter of compound: 90866-33-4

When you point to this article, it is believed that you are also very interested in this compound(90866-33-4)Reference of (R)-Ethyl 4-chloro-3-hydroxybutanoate and due to space limitations, I can only present the most important information.

Reference of (R)-Ethyl 4-chloro-3-hydroxybutanoate. Aromatic heterocyclic compounds can also be classified according to the number of heteroatoms contained in the heterocycle: single heteroatom, two heteroatoms, three heteroatoms and four heteroatoms. Compound: (R)-Ethyl 4-chloro-3-hydroxybutanoate, is researched, Molecular C6H11ClO3, CAS is 90866-33-4, about Stereochemical control of microbial reduction. 17. A method for controlling the enantioselectivity of reductions with bakers’ yeast. Author is Nakamura, Kaoru; Kawai, Yasushi; Nakajima, Nobuyoshi; Ohno, Atsuyoshi.

The stereoselectivity of the bakers’ yeast-catalyzed reduction of β-keto esters to optically active β-hydroxy esters can be controlled by introducing a 3rd reagent. To gain insight into the mechanism of this enzymic reduction, β-hydroxy ester reductases were isolated from bakers’ yeast. Four dominant competing enzymes were isolated, purified, and characterized. Among these, 2 reduced β-keto esters stereospecifically to the corresponding D-β-hydroxy esters. The other 2 afforded the L-hydroxy esters. The rates of enzymic reduction were determined in the presence and absence of the additives.

When you point to this article, it is believed that you are also very interested in this compound(90866-33-4)Reference of (R)-Ethyl 4-chloro-3-hydroxybutanoate and due to space limitations, I can only present the most important information.

Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem