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  2. Category:Five-membered rings - Wikipedia

    en.wikipedia.org/wiki/Category:Five-membered_rings

    Compounds containing rings with five atoms in them. ... Thiazoles (5 C, 126 P) Thiazolidines (1 C, 25 P) Thiazolines (1 C, 10 P) Thiolanes (8 P) Thiophenes (4 C, 130 P)

  3. Heterocyclic compound - Wikipedia

    en.wikipedia.org/wiki/Heterocyclic_compound

    A heterocyclic compound or ring structure is a cyclic compound that has atoms of at least two different elements as members of its ring(s). [1] Heterocyclic organic chemistry is the branch of organic chemistry dealing with the synthesis, properties, and applications of organic heterocycles .

  4. Hemiacetal - Wikipedia

    en.wikipedia.org/wiki/Hemiacetal

    In organic chemistry, a hemiacetal is a functional group the general formula R 1 R 2 C(OH)OR, where R 1, R 2 is a hydrogen atom or an organic substituent. They generally result from the nucleophilic addition of an alcohol (a compound with at least one hydroxy group ) to an aldehyde ( R−CH=O ) or a ketone ( R 2 C=O ) under acidic conditions.

  5. Furanose - Wikipedia

    en.wikipedia.org/wiki/Furanose

    A furanose ring structure consists of four carbon and one oxygen atom with the anomeric carbon to the right of the oxygen. The highest numbered chiral carbon (typically to the left of the oxygen in a Haworth projection ) determines whether or not the structure has a d -configuration or L -configuration.

  6. Cyclic compound - Wikipedia

    en.wikipedia.org/wiki/Cyclic_compound

    A cyclic compound or ring compound is a compound in which at least some its atoms are connected to form a ring. [1] Rings vary in size from three to many tens or even hundreds of atoms. Examples of ring compounds readily include cases where: all the atoms are carbon (i.e., are carbocycles),

  7. Pyranose - Wikipedia

    en.wikipedia.org/wiki/Pyranose

    The pyranose ring is formed by the reaction of the hydroxyl group on carbon 5 (C-5) of a sugar with the aldehyde at carbon 1. This forms an intramolecular hemiacetal . If reaction is between the C-4 hydroxyl and the aldehyde, a furanose is formed instead. [ 1 ]

  8. Tetrazole - Wikipedia

    en.wikipedia.org/wiki/Tetrazole

    A Pinner reaction of organic nitriles with sodium azide in the presence of a buffered strong acid (e.g. triethylammonium chloride) synthesizes 5-substituted 1H-tetrazoles cleanly. [10] Another method is the deamination of 5-aminotetrazole , which can be commercially obtained or prepared in turn from aminoguanidine .

  9. Category:Hemiacetals - Wikipedia

    en.wikipedia.org/wiki/Category:Hemiacetals

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