Selective 1,4-Reduction of Chalcone with Anthracene Hydride via Base-Induced Fragmentation of Their Michael Adduct

DOI: 10.1021/jo00375a042

Source and publish data:

Journal of Organic Chemistry p. 4979 - 4983 (1986)

Update date:2022-08-06

Topics:

Authors:

Stamm, Helmut

Sommer, Andreas

Onistschenko, Andreas

Woderer, Anton

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

Article abstract of DOI:10.1021/jo00375a042

Chalcone (1) and "anthracene hydride" (AH^-) form rapidly the anionic Michael adduct 2 in high yield along with the known dimerization product 5 of 1.Prolonged reaction in the presence of an excess of AH^- converts 2 into anthracene A

Full text of DOI:10.1021/jo00375a042

Products guided by the article

Product name:1-Propanone, 1,3-diphenyl-3-(9H-xanthen-9-yl)-

Cas No:105882-47-1

R&D Labs maybe for 105882-47-1

Nanjing Qirui Material Co., Ltd.

Contact:+86-25-52320053

Address:F4-5, #17 Building, Chuang Yi Yuan, No.6 Guanghua East Street, Nanjing, 210007 P.R.China
Jiangsu Seed Chem Co.,Ltd.

Contact:86-513-84128750/13773795976

Address:No.48.Youyi West Road ,Rudong Development Zone,Jiangsu Province,China
Win-Win chemical Co.Ltd

website:http://www.win-winchemical.com

Contact:0086-577-64498589

Address:6F, No. 396 Xingping Road, Longwan Industrial Zone, Wenzhou City, Zhejiang, 325000 P.R.China
Shenzhen ZheYi Chemicals Co.,LTD(Shanghai Branch)

Contact:+86-21-54159691

Address:Room1002,Building No.2, Lane 98 Bixiu Road,Minhang District, Shanghai,China 201100
Jinan Great Chemical Co.,Ltd.

Contact:+86-531-58668191 58668193 58668196 58661173

Address:No 55,Beixiaoxinzhuang West Street,Jinan City, Shandong Province

Relevant to this article

The novel macrocyclic compounds as chiral solvating agents for determination of enantiomeric excess of carboxylic acids

Doi:10.1016/j.tetasy.2008.06.012
(2008)
1,8-Naphthyridines VII. New substituted 5-amino[1,2,4]triazolo[4,3-a][1,8]naphthyridine-6-carboxamides and their isosteric analogues, exhibiting notable anti-inflammatory and/or analgesic activities, but no acute gastrolesivity

Doi:10.1016/j.ejmech.2007.10.010
(2008)
Synthesis of Sydnone Compounds Substituted by Heteroatom Groups at the 4-Positions

Doi:10.1246/bcsj.59.483
(1986)
Reactions with β-Cyanoethylhydrazine, III A New Approach for the Synthesis of Substituted 3,5-Diaminopyrazole and 1,2,4-Triazoles

Doi:10.1007/BF00809440
(1986)
Synthesis of potential Rho-kinase inhibitors based on the chemistry of an original heterocycle: 4,4-Dimethyl-3,4-dihydro-1H-quinolin-2-one

Doi:10.1016/j.ejmech.2007.11.010
(2008)
Enantioselective Henry reaction catalyzed by Cu^II salt and bipiperidine

Doi:10.1021/jo902664v
(2010)

Article Doi