Scholarly article on 3-Ethylpiperidin-4-one hydrochloride 324769-01-9 from Journal of the American Chemical Society p. 1053,1056

DOI: 10.1021/ja01210a041

Source and publish data:

Journal of the American Chemical Society p. 1053,1056 (1946)

Update date:2022-08-02

Topics:

Authors:

Stork Stork

McElvain

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

Article abstract of DOI:10.1021/ja01210a041

Full text of DOI:10.1021/ja01210a041

Products guided by the article

Product name:3-Ethylpiperidin-4-one hydrochloride

Cas No:324769-01-9

R&D Labs maybe for 324769-01-9

Changzhou Ruiping Chemical Co., Ltd

website:http://www.wishchem.com

Contact:+86-519-82324280

Address:No.288-1 Huacheng Road, Jintan
Taizhou Green Peptide Trading Co., Ltd.

Contact:--15314709780

Address:Room 1501, No71, Yuehe Road, Taizhou City, Zhejiang Province, China
Changzhou Litong Chemical Co., Ltd.

website:http://www.litonchem.com/

Contact:+86-519-86301238

Address:Laoba Rd, Hutang town Changzhou Jiangsu
DU-HOPE INTERNATIONAL GROUP

Contact:+86-25-52346955

Address:199,JIANYE ROAD,NANJING,CHINA
hangzhou verychem science and technology co.ltd

website:http://www.verypharm.com

Contact:+86-571-88162785; 88162786

Address:F1502, 753 Shenhua road, Hangzhou, China

Relevant to this article

Doi:10.1021/ja00257a049
(1987)
Allenoates in Enantioselective [2+2] Cycloadditions: From a Mechanistic Curiosity to a Stereospecific Transformation

Doi:10.1021/jacs.8b10008
(2018)
Reactions of aminoquinolines with unsaturated carboxylic acids. 3*. Synthesis of N-quinolylaspartic acids and their derivatives

Doi:10.1007/BF02256915
(2000)
Stereoselective synthesis of secondary organozinc reagents and their reaction with heteroatomic electrophiles

Doi:10.1021/ol0068400
(2001)
Dibromomethane as one-carbon source in organic synthesis: Total synthesis of (±)- and (-)-methylenolactocin

Doi:10.1016/j.tet.2005.01.057
(2005)
Cycloacylation of chloro-substituted hydroquinone dimethyl ethers with dichloromaleic anhydride

Doi:10.1007/s11172-016-1402-3
(2016)

Article Doi

DOI: 10.1021/ja01210a041