PREPARATION OF α-BROMOESTERS VIA THE HALF ESTERS OF MALONIC ACIDS A NOVEL METHOD FOR RAPID DECARBOXYLATION UNDER MILD CONDITIONS

DOI: 10.1016/S0040-4039(00)81355-6

Source and publish data:

Tetrahedron Letters p. 163 - 166 (1983)

Update date:2022-09-26

Topics:

Authors:

Goel, O. P.

Krolls, U.

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

Article abstract of DOI:10.1016/S0040-4039(00)81355-6

α-Bromomalonic acid half esters were prepared in high yield and found to be rapidly decarboxylated to α-bromoesters under mild conditions using lithium carbonate in refluxing tetrahydrofuran.

Full text of DOI:10.1016/S0040-4039(00)81355-6

Products guided by the article

Product name:Potassium; 2-ethoxycarbonyl-5-phenyl-pentanoate

Cas No:85969-95-5

R&D Labs maybe for 85969-95-5

Nanjing distinctions Medical Technology Co., Ltd.(expird)

Contact:+86-15996203785 13914714059

Address:nanjing,jiangsu , China
Foreschem Co., Ltd

Contact:+86-533-3112891

Address:zibo
Chongqing maohuan Chemicals Co., Ltd

website:http://www.bschem.com

Contact:+86 13996103726

Address:Chongqing Nan'an District Tu Town
ZHANGJIAGANG FREE TRADE ZONE YONG HAN INTERNATIONAL TRADING CO., LTD(expird)

Contact:86 512 57910558

Address:qianjin M road
Hubei Vanz Pharm Co.,Ltd

website:http://www.vanzpharm.com/en/index.html

Contact:86-27-84492310

Address:FANHU INDUSTRY PARK

Relevant to this article

Doi:10.1039/jr9540003878
(1954)
Doi:10.1021/ja00352a046
(1983)
Choline chloride/urea as a deep eutectic solvent/organocatalyst promoted three-component synthesis of 3-aminoimidazo-fused heterocycles via Groebke-Blackburn-Bienayme process

Doi:10.1016/j.tetlet.2015.12.014
(2016)
Stereoselective synthesis of premisakinolide A, the monomeric counterpart of the marine 40-membered dimeric macrolide misakinolide A

Doi:10.1021/ol050864v
(2005)
Doi:10.1080/02678370120688
(1936)
Doi:10.1021/ja01153a544
(1951)

Article Doi