The Absolute Best Science Experiment for 32780-06-6

This compound((S)-5-(Hydroxymethyl)dihydrofuran-2(3H)-one)Reference of (S)-5-(Hydroxymethyl)dihydrofuran-2(3H)-one was discussed at the molecular level, the effects of temperature and reaction time on the properties of the compound were discussed, and the optimum reaction conditions were selected.

Reference of (S)-5-(Hydroxymethyl)dihydrofuran-2(3H)-one. So far, in addition to halogen atoms, other non-metallic atoms can become part of the aromatic heterocycle, and the target ring system is still aromatic. Compound: (S)-5-(Hydroxymethyl)dihydrofuran-2(3H)-one, is researched, Molecular C5H8O3, CAS is 32780-06-6, about The conversion of racemic terminal epoxides into either (+)- or (-)-diol γ- and δ-lactones.

Epoxidation of Et 4-pentenoate and kinetic resolution of the epoxide with (R,R)-(salen)Co(OAc) complex catalyst gave Et (R)-(+)-4,5-epoxypentanoate and (S)-(+)-γ-hydroxymethyl-γ-butyrolactone in high ees. ET 5-hexenoate similarly gave Et (R)-(+)-5,6-epoxyhexanoate, (S)-(-)-5,6-dihydroxyhexanoate, and (S)-(+)-δ-hydroxymethyl-δ-valerolactone. (S)-(-)-4,5-epoxypentanoate and (R)-(-)-γ-hydroxymethyl-γ-butyrolactone were obtained by using the (S,S)-(salen)Co(OAc) complex.

This compound((S)-5-(Hydroxymethyl)dihydrofuran-2(3H)-one)Reference of (S)-5-(Hydroxymethyl)dihydrofuran-2(3H)-one was discussed at the molecular level, the effects of temperature and reaction time on the properties of the compound were discussed, and the optimum reaction conditions were selected.

Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI