Scholarly article on 2,3-diphenyl-1,2,3,4-tetrahydroquinoxaline 75960-39-3 from Journal of the American Chemical Society p. 245,247

DOI: 10.1021/ja01352a034

Source and publish data:

Journal of the American Chemical Society p. 245,247 (1931)

Update date:2022-08-04

Topics:

Authors:

Bergstrom

Ogg Ogg

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

Article abstract of DOI:10.1021/ja01352a034

Full text of DOI:10.1021/ja01352a034

Products guided by the article

Product name:2,3-diphenyl-1,2,3,4-tetrahydroquinoxaline

Cas No:75960-39-3

R&D Labs maybe for 75960-39-3

ZUNYI CITY BEI YUAN CHEMICAL CO., LTD

website:http://www.china-beiyuan.com

Contact:+86-851-27751258

Address:Shawan Town, Huichuan District, Zunyi City, Guizhou Province, China
Shanghai Taibao Pharmaceutical Technology Co., Ltd(expird)

Contact:021-52217366

Address:shanghai
Shanghai Surseechem Co.,Ltd.

Contact:+86-21-61318535

Address:Building 29,No.2139 Xizha Road, Fengxian District, Shanghai
AUSHUN PHARMACEUTICAL TECHNOLOGY CO,.LTD

Contact:+86-25-86883560 15951806178

Address:14 Dayingbi, Zhujiang Rd. East, Nanjing, Jiangsu, China.
ShanDong XinDa Chemical CO.,LTD(expird)

Contact:086-0311-87580543

Address:No.168, High Technology Development Zone Jinan Shandong China

Relevant to this article

Lewis acid mediated reactions of allyl chalcogenides with ethyl glyoxylate

Doi:10.1246/cl.2007.826
(2007)
Synthesis and inhibitory effect of novel glycyrrhetinic acid derivatives on IL-1β-induced prostaglandin E₂ production in normal human dermal fibroblasts

Doi:10.1248/cpb.53.1103
(2005)
Synthesis and characterization of in vitro and in vivo profiles of hydroxybupropion analogues: Aids to smoking cessation

Doi:10.1021/jm1003232
(2010)
Lactone Synthesis by Enantioselective Orthogonal Tandem Catalysis

Doi:10.1002/anie.201904438
(2019)
Electrospray tandem mass spectrometry analysis of methylenedioxy chalcones, flavanones and flavones

Doi:10.1002/rcm.6577
(2013)
New retinoid derivatives as back-ups of Adarotene

Doi:10.1016/j.bmc.2012.01.042
(2012)

Article Doi

DOI: 10.1021/ja01352a034