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Amine. In chemistry, amines (/ ə ˈ m iː n, ˈ æ m iː n /, [1] [2] UK also / ˈ eɪ m iː n / [3]) are compounds and functional groups that contain a basic nitrogen atom with a lone pair.Formally, amines are derivatives of ammonia (NH 3), wherein one or more hydrogen atoms have been replaced by a substituent such as an alkyl or aryl group [4] (these may respectively be called alkylamines ...
A symmetric hydrogen bond is a special type of hydrogen bond in which the proton is spaced exactly halfway between two identical atoms. The strength of the bond to each of those atoms is equal. It is an example of a three-center four-electron bond. This type of bond is much stronger than a "normal" hydrogen bond.
The polar, uncharged amino acids serine (Ser, S), threonine (Thr, T), asparagine (Asn, N) and glutamine (Gln, Q) readily form hydrogen bonds with water and other amino acids. [32] They do not ionize in normal conditions, a prominent exception being the catalytic serine in serine proteases. This is an example of severe perturbation, and is not ...
In organic chemistry, an amide, [1][2][3] also known as an organic amide or a carboxamide, is a compound with the general formula R−C (=O)−NR′R″, where R, R', and R″ represent any group, typically organyl groups or hydrogen atoms. [4][5] The amide group is called a peptide bond when it is part of the main chain of a protein, and an ...
The alpha helix is also commonly called a: Pauling–Corey–Branson α-helix (from the names of three scientists who described its structure); 3.6 13-helix because there are 3.6 amino acids in one ring, with 13 atoms being involved in the ring formed by the hydrogen bond (starting with amidic hydrogen and ending with carbonyl oxygen)
The addition of hydrogen and an amino group (NR 2) using reagents other than the amine HNR 2 is known as a "formal hydroamination" reaction. Although the advantages of atom economy and/or ready available of the nitrogen source are diminished as a result, the greater thermodynamic driving force, as well as ability to tune the aminating reagent ...
Imine. In organic chemistry, an imine (/ ɪˈmiːn / or / ˈɪmɪn /) is a functional group or organic compound containing a carbon – nitrogen double bond (C=N). The nitrogen atom can be attached to a hydrogen or an organic group (R). The carbon atom has two additional single bonds. [1][2] Imines are common in synthetic and naturally ...
Schiff bases are imines in which R 3 is an alkyl or aryl group (not a hydrogen). R 1 and R 2 may be hydrogens General structure of an azomethine compound In organic chemistry , a Schiff base (named after Hugo Schiff ) is a compound with the general structure R 1 R 2 C=NR 3 ( R 3 = alkyl or aryl , but not hydrogen ).