enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Protecting group - Wikipedia

    en.wikipedia.org/wiki/Protecting_group

    The most common protecting groups for carbonyls are acetals and typically cyclic acetals with diols. The runners-up used are also cyclic acetals with 1,2‑hydroxythiols or dithioglycols – the so-called O,S– or S,S-acetals. Ethylene glycol 1,3‑Propadiol

  3. Trimethylsilyl chloride - Wikipedia

    en.wikipedia.org/wiki/Trimethylsilyl_chloride

    TMSCl is reactive toward nucleophiles, resulting in the replacement of the chloride. In a characteristic reaction of TMSCl, the nucleophile is water, resulting in hydrolysis to give the hexamethyldisiloxane: + + The related reaction of trimethylsilyl chloride with alcohols can be exploited to produce anhydrous solutions of hydrochloric acid in alcohols, which find use in the mild synthesis of ...

  4. Acetalated dextran - Wikipedia

    en.wikipedia.org/wiki/Acetalated_dextran

    The ratio of cyclic to acyclic acetals varies with reaction time since acyclic acetals are kinetically favored and cyclic acetals are the thermodynamically favored. [5] This unique formation of cyclic and acyclic acetals leads to varying degradation time because the two acetal groups hydrolyze at different rates.

  5. Acetal - Wikipedia

    en.wikipedia.org/wiki/Acetal

    The formation of acetals reduces the total number of molecules present (carbonyl + 2 alcohol → acetal + water) and therefore is generally not favourable with regards to entropy. One situation where it is not entropically unfavourable is when a single diol molecule is used rather than two separate alcohol molecules (carbonyl + diol → acetal ...

  6. Dioxolane - Wikipedia

    en.wikipedia.org/wiki/Dioxolane

    Dioxolane is a heterocyclic acetal with the chemical formula (CH 2) 2 O 2 CH 2. It is related to tetrahydrofuran (THF) by replacement of the methylene group (CH 2) at the 2-position with an oxygen atom. The corresponding saturated 6-membered C 4 O 2 rings are called dioxanes.

  7. Trimethylsilyl group - Wikipedia

    en.wikipedia.org/wiki/Trimethylsilyl_group

    Trimethylsilyl groups on a molecule have a tendency to make it more volatile, often making the compounds more amenable to analysis by gas chromatography or mass spectrometry. An example of such trimethylsilylation is mentioned in the Brassicasterol article. Such derivatizations are often done on a small scale in special vials.

  8. Altadena winds weren't strong enough to warrant Edison ... - AOL

    www.aol.com/news/altadena-winds-were-not...

    The company's power lines ignited the Thomas fire in 2017, a Ventura and Santa Barbara County fire that killed two and created the conditions that led to a mudflow in Montecito that killed 21 people.

  9. Acetyl group - Wikipedia

    en.wikipedia.org/wiki/Acetyl_group

    The term "acetyl" was coined by the German chemist Justus von Liebig in 1839 CE to describe what he incorrectly believed to be the radical of acetic acid (the main component of vinegar, aside from water), which is now known as the vinyl group (coined in 1851 CE); "acetyl" is derived from the Latin acētum, meaning "vinegar."

  1. Related searches deprotection of a cyclic acetal gas line with solid water molecules and mass

    acetal physicsacetal reaction wikipedia