Can You Really Do Chemisty Experiments About 58081-05-3

The article 《Efficient synthesis of kinsenoside and goodyeroside A by a chemo-enzymatic approach》 also mentions many details about this compound(58081-05-3)Quality Control of (R)-4-Hydroxydihydrofuran-2(3H)-one, you can pay attention to it or contacet with the author([email protected]; [email protected]; [email protected]; [email protected]; [email protected]; [email protected]; [email protected]; [email protected]; [email protected]) to get more information.

In general, if the atoms that make up the ring contain heteroatoms, such rings become heterocycles, and organic compounds containing heterocycles are called heterocyclic compounds. An article called Efficient synthesis of kinsenoside and goodyeroside A by a chemo-enzymatic approach, published in 2014, which mentions a compound: 58081-05-3, Name is (R)-4-Hydroxydihydrofuran-2(3H)-one, Molecular C4H6O3, Quality Control of (R)-4-Hydroxydihydrofuran-2(3H)-one.

Kinsenoside (1) and goodyeroside A (2), two naturally occurring stereoisomers with diverse biol. activities, have been synthesized efficiently by a chemo-enzymic approach with a total yield of 12.7%. The aglycons, (R)- and (S)-3-hydroxy-γ-butyrolactone, were prepared from d- and l-malic acid by a four-step chem. approach with a yield of 75%, resp. These butyrolactones were then successfully glycosidated using β-D-glucosidase as a catalyst in a homogeneous organic-water system. Under the optimized enzymic conditions, the yields of kinsenoside and goodyeroside A in the enzymic steps both reached 16.8%.

The article 《Efficient synthesis of kinsenoside and goodyeroside A by a chemo-enzymatic approach》 also mentions many details about this compound(58081-05-3)Quality Control of (R)-4-Hydroxydihydrofuran-2(3H)-one, you can pay attention to it or contacet with the author([email protected]; [email protected]; [email protected]; [email protected]; [email protected]; [email protected]; [email protected]; [email protected]; [email protected]) to get more information.

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