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

Nanjing Yuance Industry&Trade Co., Ltd.

website:http://www.njyuance.cn/

Contact:+86-25-85439097

Address:B1702, Aoti Bldg, No. 130, Aoti Avenue, Nanjing, China
Jitat Company Ltd

Contact:852-27701081

Address:Room 2509, New Tech Plaza, 34 Tai Yau St., San Po Kong, HK
Shandong Yubin Chemical CO.,LTD

website:http://www.yukaichem.com/en.html

Contact:+86-536-8865336

Address:binhai economic development zone，262737 shangdong，china
ABA Chemicals (Shanghai) Limited

Contact:021- 5115 9199-232

Address:Suite 18D, #201 Ningxia Road,
Sichuan Sangao Biochemical Co., Ltd

Contact:+86-28-84874233

Address:19F, Bldg.2, Shudu Center, Tianfu 2nd St., Hi-tech zone, Chengdu 610041, Sichuan Province, 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