Substituted benzyloxyarylacetic acids: synthesis and quantitative relationships between structure and antiinflammatory activity

DOI: 10.1135/cccc19771723

Source and publish data:

Collection of Czechoslovak Chemical Communications p. 1723 - 1735 (1977)

Update date:2022-09-26

Topics:

Authors:

Kuchar Kuchar

Brunova Brunova

Rejholec

et al. et al.

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

Article abstract of DOI:10.1135/cccc19771723

Full text of DOI:10.1135/cccc19771723

Products guided by the article

Product name:Benzene, 1-chloro-2-(2-methylpropoxy)-

Cas No:60736-65-4

R&D Labs maybe for 60736-65-4

WUHAN WELLSONG INT'L CO.,LTD

Contact:+86-27-85733560

Address:NO.308,QINGNIAN RD.,WUHAN,CHINA
SunaTech Inc.

Contact:+86 512 6287 2180

Address:398 Ruoshui Road, Suzhou Industrial Park, Suzhou, Jiangsu, P. R. China
Yangling Ciyuan biotech Co., Ltd.

Contact:86-15802970736

Address:2-1804, International Park Mansion, No.2, South Fengdeng Road, Lianhu District
HANGZHOU TOYOND BIOTECH CO., LTD

Contact:+86-571-86965177

Address:No. 189, Fengqi East Road, Hangzhou, China
Nanjing distinctions Medical Technology Co., Ltd.(expird)

Contact:+86-15996203785 13914714059

Address:nanjing,jiangsu , China

Relevant to this article

PEPTIDES-XXXXI. SYNTHESIS OF THE 38-75 FRAGMENT OF A LYSOZYME ANALOGUE

Doi:10.1016/0040-4020(80)80121-9
(1980)
The reaction of Li[Al(OR)₄] R = OC(CF₃) ₂Ph, OC(CF₃)₃ with NO/NO₂ giving NO[Al(OR)₄], Li[NO₃] and N₂O. The synthesis of NO[Al(OR)₄] from Li[Al(OR)₄] and NO[SbF₆] in sulfur dioxide solution

Doi:10.1039/b405715e
(2004)
Synthesis of 3,4,5-Trisubstituted-2(3H)-thiazolethiones via Metallation of 3,4-Disubstituted-2(3H)-thiazolethiones

Doi:10.1055/s-1980-29208
(1980)
One-pot synthesis of α-bromoesters and ketones from β-ketoesters and diketones using supported reagents system

Doi:10.1016/j.tetlet.2004.01.014
(2004)
INTRODUCTION OF FURAN RING BY A NOVEL REAGENT, LITHIUM DI(3-FURYL)CUPRATE.2FURYLLITHIUM, INTO LESS REACTIVE OXIRANES

Doi:10.1016/S0040-4039(00)77859-2
(1980)
Dramatic increase of quench efficiency in "spacerless" dimaleimide fluorogens

Doi:10.1039/c0ob00455c
(2011)

Article Doi