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  2. Pyrimidine - Wikipedia

    en.wikipedia.org/wiki/Pyrimidine

    Pyrimidine (C 4 H 4 N 2; / p ɪ ˈ r ɪ. m ɪ ˌ d iː n, p aɪ ˈ r ɪ. m ɪ ˌ d iː n /) is an aromatic, heterocyclic, organic compound similar to pyridine (C 5 H 5 N). [3] One of the three diazines (six-membered heterocyclics with two nitrogen atoms in the ring), it has nitrogen atoms at positions 1 and 3 in the ring.

  3. Category:Pyrimidines - Wikipedia

    en.wikipedia.org/wiki/Category:Pyrimidines

    Pyrimidines are organic compounds that contain the pyrimidine base structure. Subcategories.

  4. Deoxyribonucleotide - Wikipedia

    en.wikipedia.org/wiki/Deoxyribonucleotide

    The nitrogenous bases are either purines or pyrimidines, heterocycles whose structures support the specific base-pairing interactions that allow nucleic acids to carry information. The base is always bonded to the 1'-carbon of the deoxyribose, an analog of ribose in which the hydroxyl group of the 2'-carbon is replaced with a hydrogen atom.

  5. Nucleotide base - Wikipedia

    en.wikipedia.org/wiki/Nucleotide_base

    Similarly, the simple-ring structure of cytosine, uracil, and thymine is derived of pyrimidine, so those three bases are called the pyrimidine bases. [ 6 ] Each of the base pairs in a typical double- helix DNA comprises a purine and a pyrimidine: either an A paired with a T or a C paired with a G.

  6. Ribonucleotide - Wikipedia

    en.wikipedia.org/wiki/Ribonucleotide

    Pyrimidine de Novo pathway. Synthesis of pyrimidine nucleotides is a much simpler process. The formation of the pyrimidine ring begins with the conversion of Aspartate to N-Carbamoylaspartate by undergoing a condensation reaction with carbamoyl phosphate. Dihydroorotase and dihydroorotase dehydrogenase then converts N-Carbamoylaspartate to orotate.

  7. Category:Fluoropyrimidines - Wikipedia

    en.wikipedia.org/wiki/Category:Fluoropyrimidines

    Fluoropyrimidines are organic compounds that contain the pyrimidine base structure. Pages in category "Fluoropyrimidines" The following 9 pages are in this category, out of 9 total.

  8. Synthesis of nucleosides - Wikipedia

    en.wikipedia.org/wiki/Synthesis_of_nucleosides

    Synthesis of nucleosides involves the coupling of a nucleophilic, heterocyclic base with an electrophilic sugar. The silyl-Hilbert-Johnson (or Vorbrüggen) reaction, which employs silylated heterocyclic bases and electrophilic sugar derivatives in the presence of a Lewis acid, is the most common method for forming nucleosides in this manner.

  9. Ribosylpyrimidine nucleosidase - Wikipedia

    en.wikipedia.org/wiki/Ribosylpyrimidine_nucleosidase

    In enzymology, a ribosylpyrimidine nucleosidase (EC 3.2.2.8) is an enzyme that catalyzes the chemical reaction. a pyrimidine nucleoside + H 2 O D-ribose + a pyrimidine base. Thus, the two substrates of this enzyme are pyrimidine nucleoside and H 2 O, whereas its two products are D-ribose and pyrimidine base.