Regioselective reactivity of some 5,7-dimethoxyindoles
摘要:
The reactivity of some 5,7-dimethoxyindoles with respect to electrophiles has been investigated. The favoured sites for reaction are C3 and C4 and regioselectivity can be controlled by the judicious arrangement of electron-withdrawing substituents. Results of formylation, acylation, the Mannich reaction, bromination and nitration are described. (c) 2005 Elsevier Ltd. All rights reserved.
Use of indole compounds for fat reduction and skin and soft tissue tightening
申请人:Alevere Medical Corporation
公开号:US10258605B2
公开(公告)日:2019-04-16
The present invention relates to indole compounds and compositions and uses thereof, including uses of the indole compounds and compositions for the reduction or removal of localized fat deposits and/or tightening of skin and soft tissue laxity in subjects. The indole compounds can be employed, for example, in the cosmetic sector or for producing pharmaceutical products.
USE OF INDOLE COMPOUNDS FOR FAT REDUCTION AND SKIN AND SOFT TISSUE TIGHTENING
申请人:Alevere Medical Corporation
公开号:EP2968272B1
公开(公告)日:2021-06-16
[EN] USE OF INDOLE COMPOUNDS FOR FAT REDUCTION AND SKIN AND SOFT TISSUE TIGHTENING<br/>[FR] UTILISATION DE COMPOSÉS D'INDOLE POUR LA RÉDUCTION DES GRAISSES ET LE RESSERREMENT DE LA PEAU ET DES TISSUS MOUS
申请人:ALEVERE MEDICAL CORP
公开号:WO2014143125A1
公开(公告)日:2014-09-18
The present invention relates to indole compounds and compositions and uses thereof, including uses of the indole compounds and compositions for the reduction or removal of localized fat deposits and/or tightening of skin and soft tissue laxity in subjects. The indole compounds can be employed, for example, in the cosmetic sector or for producing pharmaceutical products.
Regioselective reactivity of some 5,7-dimethoxyindoles
作者:Glenn C. Condie、Michelle F. Channon、Andrew J. Ivory、Naresh Kumar、David StC. Black
DOI:10.1016/j.tet.2005.03.048
日期:2005.5
The reactivity of some 5,7-dimethoxyindoles with respect to electrophiles has been investigated. The favoured sites for reaction are C3 and C4 and regioselectivity can be controlled by the judicious arrangement of electron-withdrawing substituents. Results of formylation, acylation, the Mannich reaction, bromination and nitration are described. (c) 2005 Elsevier Ltd. All rights reserved.