A SHORT SYNTHESIS OF CIS-2-FORMYL-5-HYDROXY-2-CYCLOPENTENE-1-ACETIC ACID γ-LACTONE. THE KEY INTERMEDIATE OF PROSTAGLANDIN SYNTHESIS

DOI: 10.1246/cl.1985.1057

Source and publish data:

Chemistry Letters p. 1057 - 1058 (1985)

Update date:2022-09-26

Topics:

Authors:

Sato, Masayuki

Sekiguchi, Keiko

Kaneko, Chikara

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

Article abstract of DOI:10.1246/cl.1985.1057

A practically one-pot synthesis of the title compound from 2,2-dimethyl-1,3-dioxin-4-one and cis-2-cyclopentene-1,4-diol by an application of the Mayo method is described.

Full text of DOI:10.1246/cl.1985.1057

Products guided by the article

Product name:((1S,5S)-2-Formyl-5-hydroxy-cyclopent-2-enyl)-acetic acid benzyl ester

Cas No:99930-43-5

R&D Labs maybe for 99930-43-5

Antimex Chemical Limied

website:http://www.antimex.com

Contact:0086-21-50563169

Address:Room1027,No.Jinyu Road,Pudong
Basilea Pharmaceutica China Ltd.

Contact:+86-513-82198075

Address:No.638 Xiushan Road(East),Haimen, Jiangsu 226100, P.R.China
Hangzhou Deli Chemical Co.,Ltd.

website:http://www.dlchemical.com

Contact:86 571 28006267

Address:Tangxi Industrial Area, Yuhang District, Hangzhou
Shanghai Sunway Pharmaceutical Technology Co.,Ltd.

Contact:+86-21-5161 3915

Address:Shanghai YangPu
Shijiazhuang Haotian Chemical Co., Ltd.

Contact:86-311-85044374

Address:293 Donggang Road

Relevant to this article

Doi:10.1021/jo01106a047
(1958)
Synthesis and Utilization of the Chiral Synthon Methyl 3-O-Benzyl-2,4,6-trideoxy-6-iodo-α-D-erythro-hexopyranoside in the Synthesis of a Potent HMG-CoA Reductase Inhibitor

Doi:10.1021/jo00355a014
(1986)
Doi:10.1097/00005537-200203000-00011
(1959)
Enantioselective synthesis of [1,2]-oxazinone scaffolds and [1,2]-oxazine core structures of FR900482

Doi:10.1016/j.tet.2007.07.071
(2008)
Use of comparative triazolinium triflate fragmentation rates as a tool to assay relative competency of Bronsted bases in N→N proton transfer

Doi:10.1016/j.bmcl.2009.07.067
(2009)
Doi:10.1002/hlca.19590420223
(1959)

Article Doi