Substituted tetralins VI: Tentative assignment of absolute stereochemistry of 1-methyl-1-phenyl-1,2,3,4-tetrahydro-3-naphthoic acid and N,N,1-trimethyl-1-phenyl-1,2,3,4-tetrahydro-3-naphthylamine isomers

DOI: 10.1002/jps.2600671009

Source and publish data:

Journal of Pharmaceutical Sciences p. 1367 - 1370 (1978)

Update date:2022-08-04

Topics:

Authors:

Galpin Galpin

Kandeel Kandeel

Martin Martin

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

Article abstract of DOI:10.1002/jps.2600671009

Full text of DOI:10.1002/jps.2600671009

Products guided by the article

Product name:(2S,4R)-4-Methyl-4-phenyl-1,2,3,4-tetrahydro-naphthalene-2-carboxylic acid

Cas No:68852-91-5

R&D Labs maybe for 68852-91-5

SHANGHAI SYSTEAM BIOCHEM CO., LTD

website:http://www.systeambc.com

Contact:86-021-58380978

Address:Building 87，Lane 669， Dong Jing Road Shanghai,P.R.China
Zhejiang Sanmei Chemical Industry Co., Ltd

Contact:86-579-87633213

Address:Huchu Industrial Zone, Qingnian Rd., Wuyi County, Zhejiang Prov., China.
Beijing Mediking Biopharm Co., Ltd.

Contact:+86-10-89753524/81760121/81769521

Address:Hongxianghong Incubator, Beiqijia Town, Changping district, Beijing, China
Chengdu Pukang Biotechnology Co., Ltd

website:http://www.pu-kang.com

Contact:86-028-63976226

Address:No. 868 Xiwang Road,Xinjin county,Chengdu city, China
AUSHUN PHARMACEUTICAL TECHNOLOGY CO,.LTD

Contact:+86-25-86883560 15951806178

Address:14 Dayingbi, Zhujiang Rd. East, Nanjing, Jiangsu, China.

Relevant to this article

Development of unsymmetrical dyads as potent noncarbohydrate-based inhibitors against human β-N-acetyl-D-hexosaminidase

Doi:10.1021/ml300475m
(2013)
Structure based design of macrocyclic factor XIa inhibitors: Discovery of cyclic P1 linker moieties with improved oral bioavailability

Doi:10.1016/j.bmcl.2019.08.008
(2019)
Remote C-H bond functionalization of androstane C-ring: C12-amination

Doi:10.1016/j.tetlet.2012.12.103
(2013)
Synthesis, crystal structure and antidiabetic activity of substituted (E)-3-(Benzo [d]thiazol-2-ylamino) phenylprop-2-en-1-one

Doi:10.1016/j.ejmech.2012.11.020
(2013)
An aqueous, catalyst-free and three-component synthesis of 6-amino-3-(trifluoromethyl)-1,4-dihydro-1-phenyl-4-arylpyrano[2,3-c] pyrazole-5-carbonitriles

Doi:10.1007/s11164-013-1058-7
(2014)
Potent and selective inhibition of histone deacetylase 6 (HDAC6) does not require a surface-binding motif

Doi:10.1021/jm301355j
(2013)

Article Doi