On the constitution of Mannich-bases of amides and the methyl ester of beta-resorcylic acid, gentisic acid and 3-hydroxy-naphthoic acid-(2)

DOI: 10.1002/ardp.19673001204

Source and publish data:

Archiv der Pharmazie und Berichte der Deutschen Pharmazeutischen Gesellschaft p. 992 - 1000 (1967)

Update date:2022-08-04

Topics:

Authors:

Brandes Brandes

Roth Roth

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

Article abstract of DOI:10.1002/ardp.19673001204

Full text of DOI:10.1002/ardp.19673001204

Products guided by the article

Product name:2,4-dihydroxy-3,5-bis-morpholin-4-ylmethyl-benzamide

Cas No:19045-18-2

R&D Labs maybe for 19045-18-2

Nanjing Ruizhi Industry & Technologh Co.，Ltd.

Contact:+86-25-86808110

Address:441-4-A5,NO.12 Longzang Avenue,Yuhuatai District,210039,Nanjing
Wuhan Chemwish Technology Co., Ltd

website:http://www.chemwish.com/

Contact:+86-27-67849912

Address:Room 1311, Unit 2, Block1, Innovation Road East Lake High-tech Development Zone Wuhan, Hubei，P.R. China
Jiangsu Chiatai Qingjiang Pharmaceutical Co.,Ltd

Contact:+86-517-86283327

Address:9 North Hantai Road, Huaian, China
Shanghai Forever Synthesis Co.,Ltd.

Contact:021-61124658

Address:Zhoukang Road,Pudong New District,Shanghai,China
Shanghai Biobond Pharmaceutical Co.,Ltd

website:http://www.sh-biobond.com/EnglishIndex.aspx

Contact:021-68719686 /18939786273/ 18917373795

Address:Shanghai Zhangjiang

Relevant to this article

(1S,2R)-[(benzyloxy)methyl]cyclopent-3-enol. A versatile synthon for the preparation of 4',1'a-methano- and 1',1'a-methanocarbocyclic nucleosides

Doi:10.1021/jo962124t
(1997)
Synthesis and biological evaluation of taxinine analogues as orally active multidrug resistance reversal agents in cancer

Doi:10.1016/j.bmcl.2004.06.089
(2004)
Reactions of α-Azido Sulfones with Bases

Doi:10.1021/jo01299a050
(1980)
Heterocalixarenes. 1. Calix[2]uracil[2]arene: Synthesis, X-ray Structure, Conformational Analysis, and Binding Character

Doi:10.1021/jo990085q
(1999)
O-Nitroaniline derivatives. Part 14. Cyclisations leading to benzimidazole N-oxides, N-hydroxybenzimidazolones and N-hydroxyquinoxaline-2,3-diones: A mechanistic borderline

Doi:10.1039/a607378f
(1997)
Doi:10.1016/S0008-6215(00)80059-2
()

Article Doi