A Novel Synthesis of (R)- and (S)-4-Hydroxytetrahydrofuran-2-ones

DOI: 10.1055/s-1987-28008

Source and publish data:

Synthesis p. 570 - 573 (1987)

Update date:2022-08-11

Topics:

Authors:

Tanaka, Akira

Yamashita, Kyohei

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1055/s-1987-28008

A practical synthesis of (R)- and (S)-4-hydroxytetrahydrofuran-2-ones is accomplished starting from L-ascorbic acid and D-isoascorbic acid, respectively.

Full text of DOI:10.1055/s-1987-28008

Products guided by the article

Product name:(R)-2,2-DIMETHYL-1,3-DIOXOLANE-4-ACETIC ACID, METHYL ESTER

Cas No:112031-10-4

R&D Labs maybe for 112031-10-4

Shaanxi HuaTai Bio-fine chemical company Ltd

Contact:86-029-87862197

Address:No. 5, 3rd Floor, 29 Yanta North Road, Beilin Dist.
Wuhan Silworld Chemical Co.,Ltd

website:http://www.silworldchemical.com

Contact:+86-27-85613400

Address:No.198 jiangjun Road, Wuhan,China 430033
Jiaxing Barton Chemicals

website:http://www.chinabarton.com

Contact:+86-573-82719618

Address:No. 162 Fumin Road, Honghe Town,
Wuxi Zuping Food Science And Technology Co.,LTD.

Contact:+86-510-87210822

Address:Guanlin town
Ningbo Hi-tech Zone Nice-Synth Chemical Industry Ltd.

Contact:+86-(574)-81110986

Address:No. 1210, Building 3, Wante Business Centre, Hi-tech Zone, Ningbo

Relevant to this article

Intracellular Deprotection Reactions Mediated by Palladium Complexes Equipped with Designed Phosphine Ligands

Doi:10.1021/acscatal.8b01606
(2018)
Doi:10.1016/S0040-4039(00)99984-2
(1970)
Doi:10.1246/bcsj.49.1888
(1976)
Direct benzylic functionalization of pyridines: Palladium-catalyzed mono-α-arylation of α-(2-pyridinyl)acetates with heteroaryl halides

Doi:10.1016/j.cclet.2019.06.028
(2019)
Highly enantioselective synthesis of syn- and anti-propionate aldols without diastereoselection in the chiral oxazaborolidinone-promoted aldol reaction with a silyl ketene acetal derived from ethyl 2- (methylthio)propionate

Doi:10.1016/S0957-4166(98)00159-1
(1998)
Doi:10.1021/j150575a003
(1959)

Article Doi