Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 218,393,625 papers from all fields of science
Search
Sign In
Create Free Account
4-allylphenol
Known as:
chavicol
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
2 relations
Broader (2)
Allyl Compounds
Phenols
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2017
Review
2017
Phenylpropenes: Occurrence, Distribution, and Biosynthesis in Fruit.
R. Atkinson
Journal of Agricultural and Food Chemistry
2017
Corpus ID: 206604137
Phenylpropenes such as eugenol, chavicol, estragole, and anethole contribute to the flavor and aroma of a number of important…
Expand
Highly Cited
2015
Highly Cited
2015
Modelling the effect of essential oil of betel leaf (Piper betle L.) on germination, growth, and apparent lag time of Penicillium expansum on semi-synthetic media.
Suradeep Basak
,
P. Guha
Journal of food microbiology
2015
Corpus ID: 31155941
Highly Cited
2008
Highly Cited
2008
Biosynthesis of t-Anethole in Anise: Characterization of t-Anol/Isoeugenol Synthase and an O-Methyltransferase Specific for a C7-C8 Propenyl Side Chain1[W][OA]
T. Koeduka
,
T. J. Baiga
,
J. Noel
,
E. Pichersky
Plant Physiology
2008
Corpus ID: 21452690
The phenylpropene t-anethole imparts the characteristic sweet aroma of anise (Pimpinella anisum, family Apiaceae) seeds and…
Expand
2007
2007
A pinoresinol-lariciresinol reductase homologue from the creosote bush (Larrea tridentata) catalyzes the efficient in vitro conversion of p-coumaryl/coniferyl alcohol esters into the allylphenols…
D. G. Vassão
,
Sung-jin Kim
,
Jessica K Milhollan
,
D. Eichinger
,
L. Davin
,
N. Lewis
Archives of Biochemistry and Biophysics
2007
Corpus ID: 24546635
Highly Cited
2006
Highly Cited
2006
Chavicol formation in sweet basil (Ocimum basilicum): cleavage of an esterified C9 hydroxyl group with NAD(P)H-dependent reduction.
D. G. Vassão
,
D. Gang
,
+4 authors
N. Lewis
Organic and biomolecular chemistry
2006
Corpus ID: 25607584
Propenyl- and allyl-phenols, such as methylchavicol, p-anol and eugenol, have gained importance as flavoring agents and also as…
Expand
Highly Cited
2002
Highly Cited
2002
Characterization of phenylpropene O-methyltransferases from sweet basil: facile change of substrate specificity and convergent evolution within a plant O-methyltransferase family.
D. Gang
,
N. Lavid
,
+5 authors
E. Pichersky
The Plant Cell
2002
Corpus ID: 5797393
Some basil varieties are able to convert the phenylpropenes chavicol and eugenol to methylchavicol and methyleugenol…
Expand
Highly Cited
2002
Highly Cited
2002
Differential Production of meta Hydroxylated Phenylpropanoids in Sweet Basil Peltate Glandular Trichomes and Leaves Is Controlled by the Activities of Specific Acyltransferases and Hydroxylases1
D. Gang
,
T. Beuerle
,
P. Ullmann
,
D. Werck-Reichhart
,
E. Pichersky
Plant Physiology
2002
Corpus ID: 797560
Sweet basil (Ocimum basilicum) peltate glandular trichomes produce a variety of small molecular weight phenylpropanoids, such as…
Expand
2001
2001
Volatile Components of the Essential Oils in Galanga (Alpinia officinarum Hance) from Vietnam
Tram Ngoc Ly
,
R. Yamauchi
,
Koji Kato
2001
Corpus ID: 95400967
The essential oils from fresh and dried rhizomes of galanga (Alpinia officinarum Hance) were obtained by hydro-distillation, and…
Expand
Highly Cited
2000
Highly Cited
2000
Biosynthesis of estragole and methyl-eugenol in sweet basil (Ocimum basilicum L). Developmental and chemotypic association of allylphenol O-methyltransferase activities.
E. Lewinsohn
,
Iris Ziv-Raz
,
+9 authors
Y. Shoham
Plant Science
2000
Corpus ID: 7102648
1997
1997
Oxidation of 4-alkylphenols and catechols by tyrosinase: ortho-substituents alter the mechanism of quinoid formation.
E. Krol
,
Judy L. Bolton
Chemico-Biological Interactions
1997
Corpus ID: 23478340
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