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2-chloropyrimidine

National Institutes of Health

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Pyrimidines

Papers overview

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2020
2020
Synthesis, reactivity, X-ray characterization and docking studies of N7/N9-(2-pyrimidyl)-adenine derivatives.
2017
2017
Synthesis, molecular modelling, and preliminary anticonvulsant activity evaluation of novel naphthalen-2-yl acetate and 1,6-dithia-4,9-diazaspiro [4.4] nonane-3,8-dione derivatives.
Highly Cited
2009
Highly Cited
2009
Cobalt-catalyzed cross-coupling between in situ prepared arylzinc halides and 2-chloropyrimidine or 2-chloropyrazine.
A cobalt-catalyzed cross-coupling of aryl halides with 2-chloropyrimidines or 2-chloropyrazines is reported in satisfactory to… 
2008
2008
The Auger spectroscopy of pyrimidine and halogen-substituted pyrimidines.
The C 1s and N 1s Auger spectra of pyrimidine, 2-chloropyrimidine, and 5-bromopyrimidine have been measured in an electron impact… 
2008
2008
The synthesis of potential DNA intercalaters 1. Heterocycles from the reaction of aryl bis-isothiocyanates
1,3-Bis(isoxazol-3-ylamino)benzenes, substituted on isoxazole-nitrogen with a pyrimidine group, react with triethylamine in… 
2007
2007
Comparative computational and experimental study on the thermochemistry of the chloropyrimidines.
The standard (p0 = 0.1 MPa) molar enthalpies of formation, Delta fH(0)(M), for liquid 2,4,6-trichloropyrimidine and for… 
2005
2005
Expedient parallel synthesis of 2-amino-4-heteroarylpyrimidines.
[reaction: see text] An expedient synthesis of diverse 2-amino-4-heteroarylpyrimidines via a 2-chloropyrimidine intermediate is… 
2002
2002
Photochemistry of 2-chloropyrimidine
The photochemistry of 2-chloropyrimidine (ClPy) was investigated by means of nanosecond laser flash photolysis, HPLC, mass… 
2002
2002
Palladium(0)-catalyzed enantioselective O,S-rearrangement of racemic O-allylic thiocarbamates: a new entry to enantioenriched allylic sulfur compounds.
Reaction of (+/-)-(E)-pent-3-en-2-ol, (+/-)-(E)-hept-4-en-3-ol, (+/-)-(E)-2,6-dimethylhept-4-en-3-ol, (+/-)-cyclohex-2-en-1-ol… 
2001
2001
Short and efficient syntheses of analogues of WAY-100635: new and potent 5-HT1A receptor antagonists.
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