On the lipophilicity of the 1,2-dithiole-3-thione nucleus

DOI: 10.1248/cpb.43.1894

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 1894 - 1896 (1995)

Update date:2022-08-04

Topics:

Authors:

Bona Bona

Christen

Burgot Burgot

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

Article abstract of DOI:10.1248/cpb.43.1894

Lipophilicity of the 1,2-dithiole-3-thione nucleus was studied by stepwise calculation of log P values of some dithiolethiones from fragmental lipophilic constants of suitable fragments composing the nucleus, and the results were compared with experimenta

Full text of DOI:10.1248/cpb.43.1894

NII-Electronic Library Service

Products guided by the article

Product name:methyl 2-methylthiocyclohexenyl-1-carbodithioate

Cas No:50267-85-1

R&D Labs maybe for 50267-85-1

MS( MAOSHENG )Chemical CO.,LTD

Contact:+86-519-82726678.82726378

Address:TAOXI INDUSTRY ZONE JINTAN
Jiangsu Haian Petro chemical Plant

Contact:+86-513-88902723

Address:99, Changjiang West Road, Haian County, Jiangsu
Zipont chem(wuhan）Tech co.，Ltd

Contact:+86-27-87587198

Address:wuhan
jiangsu hualin chemical co.,ltd.

Contact:86-25-87787402

Address:jaingsu,china
zhangjiagang bonded areas banggao co;ltd

website:http://www.shunchangchem.com

Contact:0086-13921972933

Address:Dongsha Chemical Zone.Zhangjiagang, Jiangsu Province

Relevant to this article

Consecutive Lossen rearrangement/transamidation reaction of hydroxamic acids under catalyst- and additive-free conditions

Doi:10.1039/c8ob00490k
(2018)
Solid-phase synthesis of core 2 O-linked glycopeptide and its enzymatic sialylation

Doi:10.1016/j.tet.2003.08.047
(2003)
A convenient one-pot synthesis of quaternary α-methoxy- and α- hydroxycarboxylic acids

Doi:10.1248/cpb.47.684
(1999)
Doi:10.1016/0031-9422(80)83019-6
(1980)
Genaral Strategies for the Synthesis of Indole Alkaloids. Total Syntheses of (+/-)-Reserpine and (+/-)-α-Yohimbine

Doi:10.1021/ja00254a036
(1987)
Synthesis and biological evaluation of chalcone, dihydrochalcone, and 1,3-diarylpropane analogs as anti-inflammatory agents

Doi:10.1016/j.bmcl.2017.02.038
(2017)

Article Doi