Synthesis and 2D QSAR of O-sulphonated β-aminols derivatives as novel antifungal and antibacterial agents
摘要:
Synthesis of a series of beta-aminol derivatives using regioselective opening reaction catalyzed by SiO2 (60-120 mesh) and O-sulphonation in THF-KOH system, comprising tert-butoxycarbonyl at secondary nitrogen and evaluate for various stains of bacteria and fungi. SAR study of synthesized compound using backward regression analysis. (C) 2011 Elsevier Ltd. All rights reserved.
EUERBY, M. R.;WAIGH, R. D., CHEM. AND IND., 1983, N 7, 287-288
作者:EUERBY, M. R.、WAIGH, R. D.
DOI:——
日期:——
US6608203B2
申请人:——
公开号:US6608203B2
公开(公告)日:2003-08-19
Synthesis and 2D QSAR of O-sulphonated β-aminols derivatives as novel antifungal and antibacterial agents
作者:Sugandha Sharma、Atindra K. Pandey、Praveen K. Shukla、Anil K. Saxena
DOI:10.1016/j.bmcl.2011.08.078
日期:2011.11
Synthesis of a series of beta-aminol derivatives using regioselective opening reaction catalyzed by SiO2 (60-120 mesh) and O-sulphonation in THF-KOH system, comprising tert-butoxycarbonyl at secondary nitrogen and evaluate for various stains of bacteria and fungi. SAR study of synthesized compound using backward regression analysis. (C) 2011 Elsevier Ltd. All rights reserved.
Tetrahydroisoquinoline compounds as estrogen agonists/antagonists
申请人:——
公开号:US20010039285A1
公开(公告)日:2001-11-08
This invention relates to compounds useful for treating or preventing obesity, breast cancer, osteoporosis, endometriosis, cardiovascular disease, prostatic disease, and the like, and to pharmaceutical composition, methods, and kits comprising such compounds.