Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 233,140,804 papers from all fields of science
Search
Sign In
Create Free Account
Pyrazines
Known as:
Pyrazines [Chemical/Ingredient]
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
50 relations
Narrower (47)
2,3,5-trimethylpyrazine
2,3-pyrazinedicarboxylic acid
2-amino-3-phenylpyrazine
2-chloropyrazine
Expand
agonists
antagonists & inhibitors
chemical synthesis
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Volatiles from the hypoxylaceous fungi Hypoxylon griseobrunneum and Hypoxylon macrocarpum
Jan Rinkel
,
Alexander Babczyk
,
Tao Wang
,
M. Stadler
,
Jeroen S. Dickschat
Beilstein Journal of Organic Chemistry
2018
Corpus ID: 54493944
The volatiles emitted by the ascomycetes Hypoxylon griseobrunneum and Hypoxylon macrocarpum (Hypoxylaceae, Xylariales) were…
Expand
2009
2009
Combinatorial Library Synthesis and Biological Evaluation of Pyrazolo[4,3‐e][1,4]diazepine as a Potential Privileged Structure
Ju-Yeon Lee
,
Yong‐Chul Kim
ChemMedChem
2009
Corpus ID: 205644899
A privileged structure: A library of tetrahydro‐1,4‐pyrazolo‐diazepin‐8(2H)‐ones was designed and synthesized to probe the…
Expand
2009
2009
A novel class of extended pi-conjugated systems: one-pot synthesis of bis-3-aminoimidazo[1,2-a]pyridines, pyrimidines and pyrazines
A. Shaabani
,
Ebrahim Soleimani
,
A. Maleki
,
Jafar Moghimirad
Molecular diversity
2009
Corpus ID: 27712215
Bis-3-aminoimidazo[1, 2-a] pyridines, pyrimidines and pyrazines as extended pi-conjugated systems were synthesized for the first…
Expand
2006
2006
Biologically Active Pyrazines of Natural and Synthetic Origin
M. Doležal
2006
Corpus ID: 103181964
In plants or insects, pyrazines play the roles of attractants, feromones and signal substances. Similar substances were found in…
Expand
2005
2005
Facile regiocontrolled synthesis of trialkyl-substituted pyrazines.
T. Elmaaty
,
L. Castle
Organic Letters
2005
Corpus ID: 40615777
[reaction: see text] Alpha-nitro ketones can be transformed selectively into trialkyl-substituted pyrazines via reaction with…
Expand
2001
2001
Dimetalation of pyrazines. a one-pot synthesis of multisubstituted pyrazine C-nucleosides.
W. Liu
,
D. Wise
,
L. Townsend
Journal of Organic Chemistry
2001
Corpus ID: 19415968
As a part of our efforts to pursue direct, convergent, and concise methodologies for the synthesis of pyrazine C-nucleosides, we…
Expand
1992
1992
Supersonic jet studies of alkyl-substituted pyrazines and pyridines. Minimum-energy conformations and torsional motion
J. I. Seeman
,
J. B. Paine
,
H. V. Secor
,
H. Im
,
E. Bernstein
1992
Corpus ID: 4987234
Conformational perferences for methyl-, ethyl-, propyl-, and isopropyl-substituted pyrazines and pyridines are determined by mass…
Expand
1991
1991
Hydrophobicity parameter of diazines. II: Analysis and prediction of partition coefficients of disubstituted pyrazines.
C. Yamagami
,
N. Takao
,
T. Fujita
Journal of Pharmacy and Science
1991
Corpus ID: 36295511
The partition coefficient in a 1-octanol-water system (log P) of a number of disubstituted pyrazines was measured. The increment…
Expand
1983
1983
Biological effects and structure-activity relationships of 1,2-dihydropyrido[3,4-b]pyrazines.
G. P. Wheeler
,
B. Bowdon
,
C. Temple
,
D. J. Adamson
,
J. Webster
Cancer Research
1983
Corpus ID: 31991763
The effects of a number of 1,2-dihydropyrido[3,4-b]pyrazines (1-deaza-7,8-dihydropteridines) upon the proliferation and the…
Expand
1980
1980
Pyrazines as marking volatiles in philanthine and nyssonine wasps (Hymenoptera: Sphecidae)
A. Borg-Karlson
,
J. Tengö
Journal of Chemical Ecology
1980
Corpus ID: 25546257
Males of several sphecid wasps apply volatile secretion on specific sites, perches. The odor is supposed to act in premating…
Expand
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