Deacetylation of N-acetylpiperdin-4-ones by a novel electrovhemical method

DOI: 10.1016/S0040-4039(00)79401-9

Source and publish data:

Tetrahedron Letters p. 3873 - 3874 (1991)

Update date:2022-08-04

Topics:

Authors:

Rajanarayanan, Arumugam

Jeyaraman, Ramasubbu

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

Article abstract of DOI:10.1016/S0040-4039(00)79401-9

A new electrochemical method for the deacetylation of N-acetylpiperidin-4-ones, in benzene-methanol mixture containing sodium hydroxide, has been developed. Carbonyl group in the ring is not affected.

Full text of DOI:10.1016/S0040-4039(00)79401-9

Products guided by the article

Product name:4-Piperidinol, 2,6-diphenyl-

Cas No:2403-90-9

R&D Labs maybe for 2403-90-9

hangzhou verychem science and technology co.ltd

website:http://www.verypharm.com

Contact:+86-571-88162785; 88162786

Address:F1502, 753 Shenhua road, Hangzhou, China
HANGZHOU FOREWIN PHARMA CO., LTD

Contact:+86-571-89053961

Address:hangzhou
Shanghai Send Pharmaceutical Technology Co., Ltd.

website:http://www.shsendpharma.com

Contact:021-58088081, +8613585868794

Address::Room A601, Building 1,NO. 800 Qingdai Road Pudong District Shanghai,China
miao tie sheng

Contact:0311-13263231263

Address:jian hua street,Shijiazhuang City, China
Hangzhou Sartort Biopharma Co., Ltd

website:http://www.sartort.com

Contact:86-571-87039693

Address:No. 57, Tech Park Road, Hangzhou, Zhejiang, China

Relevant to this article

Synthetic study of pinnatoxin A: Intramolecular Diels-Alder approach to the AG-ring

Doi:10.1055/s-1999-2743
(1999)
Aminomethylation of Afromosin, Cladrastin, and Their 2-Methyl Derivatives

Doi:10.1007/s10600-018-2440-x
()
Syntheses and properties of chiral pentahomothiazacalix[3]arenes

Doi:10.1002/jhet.5570350614
(1998)
Doi:10.1021/jo00831a116
(1970)
Doi:10.1007/BF00609040
(1964)
Synthesis of pyrrolidine or piperidine ring-fused azepino[5,4,3- cd]indole derivatives

Doi:10.1016/S0040-4039(99)01076-X
(1999)

Article Doi