Results 281 to 290 of about 121,011 (315)
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Pyrimidines. XIII. Novel pyrimidine to pyrimidine transformation reactions

Journal of Heterocyclic Chemistry, 1977
AbstractNovel pyrimidine to pyrimidine transformation reactions are described. 1,3‐Dimethyl‐(or diethyl)‐uracil(1) are converted into isocytosine, 2‐thiouracil or uracil derivatives by treatment with guanidine, thiourea or urea, respectively. The latter two cases require base catalysis. The effects of some substituents at C‐5 and C‐6 of 1,3‐dialkylated
Kyoichi A. Watanabe   +2 more
openaire   +2 more sources

The Auger spectroscopy of pyrimidine and halogen-substituted pyrimidines

The Journal of Chemical Physics, 2008
The C 1s and N 1s Auger spectra of pyrimidine, 2-chloropyrimidine, and 5-bromopyrimidine have been measured in an electron impact experiment at 1000 eV. In the case of the halogen-substituted pyrimidines, also the Cl 2p and Br 3d Auger spectra have been recorded.
Storchi L   +5 more
openaire   +4 more sources

Synthetic chemistry of pyrimidines and fused pyrimidines: A review [PDF]

open access: possibleSynthetic Communications, 2016
AbstractReview: 100 refs.
Selvaraj Mohana Roopan, Rajesh Sompalle
openaire   +2 more sources

ChemInform Abstract: Synthesis of Novel Carbazoyl‐Linked Pyrimidine—Pyrimidine and Pyrimidine—Purine Dinucleotide Analogues.

ChemInform, 1999
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Susana Fernández   +3 more
openaire   +3 more sources

Anticancer pyrimidines, pyrimidine nucleosides and prodrugs

1990
Of the plethora of pyrimidines, pyrimidine nucleosides, analogues and prodrug derivatives that have been synthesised and evaluated as anticancer agents, only two are in general clinical use. The long-studied 5-fluorouracil (5-FUra (1), see Scheme 9.1), and some nucleoside and prodrug derivatives, are used regularly for the treatment of breast cancer ...
M. J. Robins, M. MacCoss
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New Pyrimidine Pathway involved in the Biosynthesis of the Pyrimidine of Thiamine [PDF]

open access: possibleNature, 1967
OUR, studies with mutants of Salmonella typhimurium LT2 have revealed that the pyrimidine moiety of thiamine is synthesized by a new biosynthetic route using intermediates from the purine biosynthetic pathway. Radioactive labelling has indicated that the conventional nucleic acid pyrimidine biosynthetic pathway is not used for biosynthesis of the ...
Peter C. Newell, R. G. Tucker
openaire   +2 more sources

Pyrimidines as block units in heterocycles: novel synthesis of pyrimidines and condensed pyrimidine derivatives

Journal of the Iranian Chemical Society, 2019
Compound 1 condensed with benzaldehyde to produce styryl pyrimidine 2. Pyridopyrimidines 5, 8 and 10 resulted from [4 + 2] cycloaddition (condensation) of 1 with malononitrile, ethyl cyanoacetate and/or ethyl acetoacetate. Compound 1 was also concerted to pyridopyrimidine 14 through multistep reaction (hydrolysis, chlorination, isothiocyanate formation
Hamed Y. Moustafa   +4 more
openaire   +2 more sources

Receptors for Purines and Pyrimidines

Pharmacological Reviews, 1998
### A. Overview Extracellular purines (adenosine, ADP, and ATP) and pyrimidines (UDP and UTP) are important signaling molecules that mediate diverse biological effects via cell-surface receptors termed purine receptors.
Vera Ralevic, Geoffrey Burnstock
openaire   +3 more sources

Purines and Pyrimidines

1987
Nucleic acids are comprised of nitrogenous bases (purines and pyrimidines), pentose sugars (ribose and deoxyribose) and phosphate groups. Specific sequences of purines and pyrimidines encode the genetic information of cells and organisms.
openaire   +2 more sources

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