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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

    العربية; Беларуская; Български; Bosanski; Català; Čeština; Deutsch; Ελληνικά; Español; Esperanto; Euskara; فارسی; Français

  4. List of islands of Greece - Wikipedia

    en.wikipedia.org/wiki/List_of_islands_of_Greece

    Regions of the Greek islands. Greece has many islands, [Note 1] with estimates ranging from somewhere around 1,200 [1] to 6,000, [2] depending on the minimum size to take into account. The number of inhabited islands is variously cited as between 166 [3] and 227. [2] The largest Greek island by both area and population is Crete, located at the ...

  5. Purine - Wikipedia

    en.wikipedia.org/wiki/Purine

    Purine is a heterocyclic aromatic organic compound that consists of two rings (pyrimidine and imidazole) fused together. It is water-soluble. Purine also gives its name to the wider class of molecules, purines, which include substituted purines and their tautomers. They are the most widely occurring nitrogen-containing heterocycles in nature. [1]

  6. Fluoropyrimidine - Wikipedia

    en.wikipedia.org/wiki/Fluoropyrimidine

    Left: The structure of pyrimidine with the locants for ring atoms marked. Right : 5-Fluorouracil , a fluoropyrimidine formally named as 5-fluoro-1 H ,3 H -pyrimidine-2,4-dione Fluoropyrimidines are a general class organic compounds in which the substituent (s) around a pyrimidine ring include at least one fluorine atom.

  7. Pyrimidone - Wikipedia

    en.wikipedia.org/wiki/Pyrimidone

    Pyrimidone is the name given to either of two heterocyclic compounds with the formula C 4 H 4 N 2 O: 2-pyrimidone and 4-pyrimidone. The compounds can also be called 2-hydroxypyrimidine or 4-hydroxypyrimidine respectively, based on a substituted pyrimidine , or 1,3- diazine , ring.

  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. Imidazopyridine - Wikipedia

    en.wikipedia.org/wiki/Imidazopyridine

    Imidazo[1,2-a]pyridine—an example of imidazopyridine and a core structure of zolpidem and some compounds described below.. An imidazopyridine is a nitrogen containing heterocycle that is also a class of drugs that contain this same chemical substructure.