Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 221,894,032 papers from all fields of science
Search
Sign In
Create Free Account
Resorcinols
Known as:
meta-Dihydroxybenzenes
, m-Dihydroxybenzenes
, Resorcinols [Chemical/Ingredient]
Expand
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
50 relations
Narrower (46)
12-hydroxyhidroresorcylide
13-hydroxyhidroresorcylide
2-methylresorcinol
2-n-hexyl-5-n-propylresorcinol
Expand
In Blood
agonists
antagonists & inhibitors
chemical synthesis
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Regioselective, cascade [3+2] annulation of β-naphthols (resorcinols) with Z-enoate propargylic alcohols: a novel entry for the synthesis of complex naphtho(benzo)furans.
Prabhakararao Tharra
,
Beeraiah Baire
Chemical Communications
2016
Corpus ID: 35479720
An acid promoted, unprecedented cascade [3+2] annulation strategy for the synthesis of complex naphtho- and benzofurans is…
Expand
Review
2011
Review
2011
Cell signaling and receptors with resorcinols and flavonoids: redox, reactive oxygen species, and physiological effects
P. Kovacic
,
R. Somanathan
Journal of Receptor and Signal Transduction…
2011
Corpus ID: 5279054
There have been appreciable numbers of reviews on monophenols, catechols, and hydroquinones. However, the resorcinol class has…
Expand
Review
2010
Review
2010
Mechanistic studies of tyrosinase suicide inactivation
C. Ramsden
,
P. Riley
2010
Corpus ID: 102184777
Tyrosinase is a copper containing enzyme that oxidises both phenols and catechols to ortho- quinones. The oxidation of catechols…
Expand
2010
2010
Pericyclic reaction of a zwitterionic salt of an enedione-diazoester. A novel strategy for the synthesis of highly functionalized resorcinols.
Yu Liu
,
K. Bakshi
,
P. Zavalij
,
M. Doyle
Organic Letters
2010
Corpus ID: 22366693
Enedione-diazoesters formed from 3-TBSO-2-diazo-3-butenoates undergo base-catalyzed pericyclization that with dinitrogen…
Expand
2005
2005
Synthesis of 2,3-dihydro-3-hydroxy-2-hydroxylalkylbenzofurans from epoxy aldehydes. One-step syntheses of brosimacutin G, vaginidiol, vaginol, smyrindiol, xanthoarnol, and Avicenol A. Biomimetic…
Y. Zou
,
M. Lobera
,
B. Snider
Journal of Organic Chemistry
2005
Corpus ID: 9098853
We have developed two practical one-step syntheses of 2,3-dihydro-3-hydroxy-2-hydroxyalkylbenzofurans from readily available…
Expand
2002
2002
Nematicidal alkylene resorcinols from Lithraea molleoides.
S. Valcic
,
G. Wächter
,
C. Eppler
,
B. Timmermann
Journal of Natural Products
2002
Corpus ID: 6784133
Four new alkylene resorcinols, (Z,Z)-5-(trideca-4,7-dienyl)resorcinol (1), (Z,Z,Z)-5-(trideca-4,7,10-trienyl)resorcinol (2), (Z,Z…
Expand
Highly Cited
2000
Highly Cited
2000
Inhibition of Tyrosinase by Flavonoids, Stilbenes and Related 4-Substituted Resorcinols: Structure-Activity Investigations
Kuniyoshi Shimizu
,
Ryuichiro Kondo*, and
,
K. Sakai
Planta Medica
2000
Corpus ID: 20569124
Artocarpus incisus
Highly Cited
1997
Highly Cited
1997
Simple Synthesis of 5-Substituted Resorcinols: A Revisited Family of Interesting Bioactive Molecules.
E. Alonso
,
D. Ramón
,
M. Yus
Journal of Organic Chemistry
1997
Corpus ID: 20298714
The reaction of 3,5-dimethoxybenzyl trimethylsilyl ether (3) with different aldehydes (n-PrCHO, n-C(11)H(23)CHO, MeCHO, PhCHO) in…
Expand
1987
1987
The effect of 5-(n-alk(en)yl)resorcinols on membranes. II. Dependence of the aliphatic chain length and unsaturation.
A. Kozubek
Acta Biochimica Polonica
1987
Corpus ID: 20933077
The effect of chain length and unsaturation on the haemolytic properties of cereal resorcinolic lipids, (5-n-alk(en)ylresorcinols…
Expand
1985
1985
Allergenic 5-alkyl- and 5-alkenylresorcinols from philodendron species
Torsten Reffstrup
,
P. Boll
1985
Corpus ID: 98128968
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE