10366-19-5Relevant academic research and scientific papers
STRUCTURE-FUNGICIDAL PROPERTIES OF SOME 3- AND 4-HYDROXYLATED STILBENES AND BIBENZYL ANALOGUES
Schultz, T. P.,Boldin, W. D.,Fisher, T. H.,Nicholas, D. D.,McMurtrey, K. D.,Pobanz, K.
, p. 3801 - 3806 (1992)
The fungicidal activity of some substituted hydroxylated stilbenes and bibenzyls was measured against three wood-destroying fungi using the agar plate technique.Four 3-hydroxystilbene derivatives and 3-hydroxybibenzyl were active against the white-rot fun
Prevention of Marine Biofouling Using the Natural Allelopathic Compound Batatasin-III and Synthetic Analogues
Moodie, Lindon W. K.,Trepos, Rozenn,Cervin, Gunnar,Brathen, Kari Anne,Lindgard, Bente,Reiersen, Rigmor,Cahill, Patrick,Pavia, Henrik,Hellio, Claire,Svenson, Johan
supporting information, p. 2001 - 2011 (2017/08/04)
The current study reports the first comprehensive evaluation of a class of allelopathic terrestrial natural products as antifoulants in a marine setting. To investigate the antifouling potential of the natural dihydrostilbene scaffold, a library of 22 syn
Synthesis of 1-(3,4-dihydroxy-5-nitrophenyl)-2-phenyl-ethanone and derivatives as potent and long-acting peripheral inhibitors of catechol-O-methyltransferase
Learmonth, David A.,Vieira-Coelho, Maria A.,Benes, Jan,Alves, Paula C.,Borges, Nuno,Freitas, Ana P.,Soares-da-Silva, Patrício
, p. 685 - 695 (2007/10/03)
A homologous series of novel nitro-catechol structures (7a-7e) were synthesized and tested as inhibitors of the enzyme catechol-O-methyltransferase (COMT). Increasing chain length was found to have significant impact on both brain penetration and duration
Preparation of 3,4-Dihydroxy-1-benzeneethanol: A Reinvestigation
Baraldi, Pier Giovanni,Simoni, Daniele,Manfredini, Stefano,Menziani, Emilia
, p. 684 - 686 (2007/10/02)
A reinvestigation of the two known methods of preparation of the title compound 1 revealed that one of these leads to a mixture of 1 and 4--1,2-benzenediol (5).The other method yields only 2-methoxy-4-(2-phenylethyl)phenol (6).An unambiguous straightforward preparation of 1 by LiAlH4 reduction of 3,4-dihydroxy-1-benzeneacetic acid (8) is described.
