FIRST SYNTHESIS OF 40IMIDAZOLIDINONE

DOI: 10.3987/R-1986-01-0025

Source and publish data:

Heterocycles p. 25 - 28 (1986)

Update date:2022-08-02

Topics: Synthesis Yield Catalyst Reactants Purification

Authors:

Nitta, Yoshihiro

Yamaguchi, Tamie

Tanaka, Toshiko

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

Article abstract of DOI:10.3987/R-1986-01-0025

First synthesis of 4-imidazolidinone has been achieved via Beckman rearrangement of 1-alkoxycarbonylazetidin-3-one oxime sulfonates with alumina, followed by removal of the alkoxycarbonyl groups.

Full text of DOI:10.3987/R-1986-01-0025

Products guided by the article

Product name:N-ethoxycarbonyl-glycine amide

Cas No:105259-02-7

R&D Labs maybe for 105259-02-7

Jiande City Silibase Silicone New Material Manufacture Co., Ltd.

Contact:15967177856

Address:Genglou Industrial Development Area
Melone Pharmaceutical Co., ltd

Contact:+86-411 82593920, 82593631

Address:No 232, JInma Roda, Development Zone, Dalian, China
Compro Shijiazhuang Fine Chemical Co., Ltd

Contact:0086-311-89689838

Address:Economic and Technological Development Zone of Shijiazhuang,Hebei
Wuxi Zuping Food Science And Technology Co.,LTD.

Contact:+86-510-87210822

Address:Guanlin town
Tianjin Emulsion Science&Technology Development Co.,Ltd

Contact:13901380442

Address:Vake Garden New Town New Yi Bai Road Beichen District Tianjin,China

Relevant to this article

13C NMR Study of Substituted 10,10-Diphenyl-9-Phenanthrones. Structure Determination and Signal Assignment using 2D NMR Techniques

Doi:10.1002/mrc.1260271205
(1989)
Total synthesis of mycalamide a and 7-epi-mycalamide A

Doi:10.1021/ol005629l
(2000)
Medicinal foodstuffs. II. On the bioactive constituents of the tuber of Sagittaria trifolia L. (Kuwai, Alismataceae): Absolute stereostructures of trifoliones A, B, C, and D, sagittariosides a and b, and arabinothalictoside

Doi:10.1248/cpb.44.492
(1996)
Readily available unprotected amino aldehydes

Doi:10.1021/ja065898s
(2006)
Rearrangement of ethers: A new route to tolterodine

Doi:10.1080/00397911.2010.488308
(2011)
Asymmetric Synthesis of (5R,6S)-6-Acetoxy-5-hexadecanolide, the Major Component of the Oviposition Attractant Pheromone of the Mosquito Culex pipens fatigans, and Two of Its Stereoisomers

Doi:10.1021/jo00376a056
(1986)

Article Doi