KERATIN DYEING COMPOUNDS, KERATIN DYEING COMPOSITIONS CONTAINING THEM, AND USE THEREOF
申请人:The Procter and Gamble Company
公开号:EP1781241A1
公开(公告)日:2007-05-09
[EN] 2-(AMINO OR SUBSTITUTED AMINO)-3-5-6-SUBSTITUTED PHENOL COMPOUNDS, DYEING COMPOSITIONS CONTAINING THEM, AND USE THEREOF<br/>[FR] COMPOSES DE PHENOL 3-5-6-SUBSTITUE 2-(AMINO OU AMINO-SUBSTITUE), COMPOSITIONS DE TEINTURE LES CONTENANT ET USAGE ASSOCIE
申请人:PROCTER & GAMBLE
公开号:WO2006023438A1
公开(公告)日:2006-03-02
The present invention relates to 2-(amino or substituted amino)-3, 5, 6-substituted phenol compounds according to the Formula (I), as defined herein and compositions for the oxidative dyeing of keratin fibres, omprising a medium suitable for dyeing and a compound of the Formula (I).
[EN] KERATIN DYEING COMPOUNDS, KERATIN DYEING COMPOSITIONS CONTAINING THEM, AND USE THEREOF<br/>[FR] COMPOSES COLORANTS A BASE DE KERATINE, COMPOSITIONS COLORANTES LES CONTENANT ET LEUR UTILISATION
申请人:PROCTER & GAMBLE
公开号:WO2006026488A1
公开(公告)日:2006-03-09
Compositions for the oxidative dyeing of keratin fibers, comprising a medium suitable for dyeing and at least one 5-membered aza heteroaromatic keratin dyeing compound with an N-hydroxy or N-amino group and derivatives thereof. A method for oxidative dyeing of keratin fibers, comprising applying such compositions in the presence of an oxidizing agent, for a period sufficient to develop the desired coloration.
[EN] INHIBITORS OF ACETYL-COA CARBOXYLASE<br/>[FR] INHIBITEURS DE L'ACÉTYL-COA CARBOXYLASE
申请人:FOREST LAB HOLDINGS LTD
公开号:WO2010127208A1
公开(公告)日:2010-11-04
The present invention relates to compounds that act as acetyl-CoA carboxylase (ACC) inhibitors. The invention also relates to methods of preparing the compounds, compositions containing the compounds, and to methods of treatment using the compounds.
Bioinspired Selective Synthesis of Heterodimer 8–5′ or 8–<i>O</i>–4′ Neolignan Analogs
作者:Kui Dong、Chuang-Yuan Zhao、Xiao-Ju Wang、Li-Zhu Wu、Qiang Liu
DOI:10.1021/acs.orglett.1c00762
日期:2021.4.2
The bioinspired synthesis of heterodimer neolignan analogs is reported by single-electron oxidation of both alkenyl phenols and phenols individually, followed by a combination of the resultant radicals. This oxidative radical cross-coupling strategy can afford heterodimer 8–5′ or 8–O–4′ neolignan analogs selectively with the use of air as the terminal oxidant and copper acetate as the catalyst at room