Scholarly article on 1-(2-Nitro-5-benzyloxybenzal)-2-methyl-1,2,3,4-tetrahydro-isochinolin 17121-83-4 from Journal of Pharmaceutical Sciences p. 1441,1445

DOI: 10.1002/jps.2600561114

Source and publish data:

Journal of Pharmaceutical Sciences p. 1441,1445 (1967)

Update date:2022-08-03

Topics:

Authors:

Sam Sam

Bej Bej

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

Article abstract of DOI:10.1002/jps.2600561114

Full text of DOI:10.1002/jps.2600561114

Products guided by the article

Product name:1-(2-Nitro-5-benzyloxybenzal)-2-methyl-1,2,3,4-tetrahydro-isochinolin

Cas No:17121-83-4

R&D Labs maybe for 17121-83-4

HUNAN CHEMAPI BIOLOGICAL TECHNOLOGY CO.,LTD.

Contact:+86-186-02659358

Address:1004, building 3, Wanke Jinsemaitianyuan, 498 Guitang Road, Yuhua District, Changsha City, Hunan Province, China
GLD peptide scientific lnc.

Contact:21-7631221 15884421033

Address:326 Science and technology,Shanghai,China
Jiangxi Biochem Co.,Ltd

Contact:86-791-86629460

Address:1-6F, 118 Xinzhou road, Nanchang, Jiangxi, China
H&Y International Group Ltd

Contact:+86-571-86491666

Address:SHI XIANG ROAD
Tianjin Realet Chemical Technology Co.,Ltd.

website:http://www.realetchem.com

Contact:+86-022-58788819

Address:shuanggang industrial park

Relevant to this article

About a practical synthesis of Ambrox from sclareol: A new preparation of a ketone key intermediate and a close look at its Baeyer-Villiger oxidation

Doi:10.1002/hlca.200490239
(2004)
Synthesis of Carboxylated Pyrrolidine Derivatives via 1,3-Dipolar Cycloadditions of Homochiral Double-Stabilised E-Azomethine Ylids.

Doi:10.1016/0957-4166(95)00198-X
(1995)
Homologues of anti-HIV active isodideoxynucleosides

Doi:10.1016/0040-4020(95)00626-J
(1995)
A Tunable and Enantioselective Hetero-Diels–Alder Reaction Provides Access to Distinct Piperidinoyl Spirooxindoles

Doi:10.1002/anie.201708355
(2017)
Syntheses of [5,8-¹³C₂]- and [1,12-¹³C₂]spermine using potassium [¹³C]cyanide as the ¹³C source

Doi:10.1248/cpb.43.2001
(1995)
Addition of electrophiles to unsymmetric alkenes. Effects of β oxygen substituents on the stereo- and regio-chemistry of positive halogen addition

Doi:10.1039/a801001c
(1998)

Article Doi

DOI: 10.1002/jps.2600561114