Synthesis of Disodium Prephenate

DOI: 10.1039/c39840001008

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 1008 - 1010 (1984)

Update date:2022-08-03

Topics:

Authors:

Ramage, Robert

MacLeod, Angus M.

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

Article abstract of DOI:10.1039/c39840001008

An efficient synthesis of disodium prephenate has been achieved utilising a 5-ylidene-1,3-dioxolan-4-one intermediate as a protected α-keto acid.

Full text of DOI:10.1039/c39840001008

View Article Online / Journal Homepage / Table of Contents for this issue

View Article Online

Products guided by the article

Product name:6-Methoxy-4-oxo-1-[3-oxo-1,4-dioxa-spiro[4.5]dec-(2Z)-ylidenemethyl]-cyclohex-2-enecarboxylic acid methyl ester

Cas No:110115-70-3

R&D Labs maybe for 110115-70-3

Shenzhen JYMed Technology Co.,Ltd.

website:http://www.jymedtech.com

Contact:+86-755-26612112

Address:1#8,9/F, Biomedicine innovation Industrial Park, No.14, Jinhui Road, Pingshan Sistrict, Shenzhen, China
Shanghai Korey Pharm Co.,Ltd.(expird)

Contact:021-61840961 021-61840962

Address:No.157,Zhuguang Rd, Qingpu, Shanghai, China
Jiangsu Dacheng Pharmaceutical and Chemical Co.,Ltd

Contact:+86-0517-87036900

Address:Chuzhou Chemical park, Huai'an, Jiangsu Province
WEIFANG RICHEM INTERNATIONAL LTD

Contact:86-536-2222176

Address:weifang,shandong
Zhengzhou Institute of Chiral Pharmer Research Co., Ltd.

Contact:86-371-55219111

Address:15 Floor, 2 Building, Central China Technovalley, Zhongyuan West Road

Relevant to this article

An Improved Synthesis of (-)-(1R,2S,3R,4S)-2-Benzyloxy-3-bornanol (12) on a Preparative Scale

Doi:10.1055/s-1986-31783
(1986)
IODINATION OF ALKYLBENZENES WITH IODINE AND SILVER NITRITE

Doi:10.1016/S0040-4039(01)80650-X
(1989)
Tandem β-enamino ester formation and cyclization with o-alkynyl anilines catalyzed by InBr₃: Efficient synthesis of β-(N-Indolyl)-α,β-unsaturated esters

Doi:10.1021/jo802435b
(2009)
A versatile catalyst for reductive animation by transfer hydrogenation

Doi:10.1002/anie.201002944
(2010)
SYNTHESIS OF BOTH THE ENANTIOMERS OF LARDOLURE, THE AGGREGATION PHEROMONE OF THE ACARID MITE, LARDOGLYPHUS KONOI

Doi:10.1016/S0040-4020(01)88157-6
(1986)
Doi:10.1021/jo01066a014
(1961)

Article Doi