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  2. Oxazolidine - Wikipedia

    en.wikipedia.org/wiki/Oxazolidine

    Oxazolidine is a five-membered heterocycle ringwith the formula (CH 2) 3 (NH)O.The O atom and NH groups are not mutually bonded, in contrast to isoxazolidine. [ 2 ] [ 3 ] Oxazolidines (emphasis on plural) are derivatives of the parent oxazolidine owing to the presence of substituents on carbon and/or nitrogen.

  3. Oxazoline - Wikipedia

    en.wikipedia.org/wiki/Oxazoline

    2‑oxazoline, 3‑oxazoline, and 4‑oxazoline (from left to right) Three structural isomers of oxazoline are possible depending on the location of the double bond, however only 2‑oxazolines are common. 4‑Oxazolines are formed as intermediates during the production of certain azomethine ylides [2] but are otherwise rare. 3‑Oxazolines are even less common but have been synthesised ...

  4. Oxazole - Wikipedia

    en.wikipedia.org/wiki/Oxazole

    In the Cornforth rearrangement of 4-acyloxazoles is a thermal rearrangement reaction with the organic acyl residue and the C5 substituent changing positions. Various oxidation reactions. One study [ 7 ] reports on the oxidation of 4,5-diphenyloxazole with 3 equivalents of CAN to the corresponding imide and benzoic acid :

  5. List of aminorex analogues - Wikipedia

    en.wikipedia.org/wiki/List_of_aminorex_analogues

    This is a list of aminorex analogues. Aminorex itself is a stimulant drug with a 5-phenyl-2-amino-oxazoline structure. It was developed in the 1960s as an anorectic, [1] [2] [3] but withdrawn from sale after it was discovered that extended use produced pulmonary hypertension, often followed by heart failure, which resulted in a number of deaths. [4]

  6. 2-Oxazolidinone - Wikipedia

    en.wikipedia.org/wiki/2-oxazolidinone

    [4] Nine years later Gabriel returned to the topic together with G. Eschenbach, developing a more efficient synthesis using sodium bicarbonate instead of the silver salt. They referred to the compound as "Oxäthylcarbaminsäureanhydrid" (hydroxyethylcarbamic acid anhydride), recognizing its relationship to ethanolamine and its cyclic structure.

  7. Substituted phenylmorpholine - Wikipedia

    en.wikipedia.org/wiki/Substituted_phenylmorpholine

    Substituted phenylmorpholines, or substituted phenmetrazines alternatively, are chemical derivatives of 2-phenylmorpholine or of the psychostimulant drug phenmetrazine.Most such compounds act as releasers of monoamine neurotransmitters, and have stimulant effects.

  8. Diphenylmethane - Wikipedia

    en.wikipedia.org/wiki/Diphenylmethane

    Diphenylmethane is an organic compound with the formula (C 6 H 5) 2 CH 2 (often abbreviated CH 2 Ph 2). The compound consists of methane wherein two hydrogen atoms are replaced by two phenyl groups. It is a white solid. Diphenylmethane is a common skeleton in organic chemistry. The diphenylmethyl group is also known as benzhydryl.

  9. 3,4-Dimethoxyphenethylamine - Wikipedia

    en.wikipedia.org/wiki/3,4-Dimethoxyphenethylamine

    3,4-Di methoxy phenethylamine (DMPEA) is a chemical compound of the phenethylamine class. It is an analogue of the major human neurotransmitter dopamine where the 3- and 4-position hydroxy groups have been replaced with methoxy groups. It is also closely related to mescaline which is 3,4,5-trimethoxyphenethylamine and to 3,4 ...