2(3H)-Furanone, dihydro-3-phenyl-, (3R)-

Base Information

Chemical Name:2(3H)-Furanone, dihydro-3-phenyl-, (3R)-
CAS No.:112607-27-9
Molecular Formula:C10H10O2
Molecular Weight:162.188
Hs Code.:

Synonyms:

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Chemical Property of 2(3H)-Furanone, dihydro-3-phenyl-, (3R)-

Chemical Property:

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Technology Process of 2(3H)-Furanone, dihydro-3-phenyl-, (3R)-

There total 10 articles about 2(3H)-Furanone, dihydro-3-phenyl-, (3R)- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 879098-62-1
(2R,3R)-2-{(+)-isomenthoxy}-3-phenyl-1-oxacyclopentane

: 112607-27-9
(R)-α-Phenyl-γ-butyrolactone

Guidance literature:: With jones reagent; In acetone; at 20 ℃; for 1h;
DOI:10.1021/ja057560o

Reference yield:

: 1131-15-3,112489-85-7
2-phenylsuccinic anhydride

: 1008-73-7,68844-05-3,93601-84-4,68844-04-2
(R)-4-phenyl-4,5-dihydrofuran-2(3H)-one

: 68844-05-3
4-phenyldihydrofuran-2-one

: 112607-26-8
(S)-α-Phenyl-γ-butyrolactone

: 112607-27-9
(R)-α-Phenyl-γ-butyrolactone

Guidance literature:: 2-phenylsuccinic anhydride; With 2,2,2-trifluoroethanol; modified cinchona alkaloid (DHQD)2AQN; In diethyl ether; at -24 ℃;

With lithium triethylborohydride; In tetrahydrofuran; at 0 ℃; for 0.416667h; Further stages.;
DOI:10.1021/ja011766h

Reference yield:

: C₁₀H₉BrO₂

: 112607-26-8
(S)-α-Phenyl-γ-butyrolactone

: 112607-27-9
(R)-α-Phenyl-γ-butyrolactone

Guidance literature:: With D-glucose; glucose dehydrogenase GDH-105; alcohol dehydrogenase from Ralstonia species; nicotinamide adenine dinucleotide phosphate; glycerol; calcium chloride; In dimethyl sulfoxide; at 25 ℃; for 12h; pH=7; Overall yield = 82 %; enantioselective reaction; Irradiation; Enzymatic reaction;
DOI:10.1038/nature20569