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  2. N-Hydroxysuccinimide - Wikipedia

    en.wikipedia.org/wiki/N-Hydroxysuccinimide

    N-Hydroxysuccinimide (NHS) is an organic compound with the formula (CH 2 CO) 2 NOH. It is a white solid that is used as a reagent for preparing active esters in peptide synthesis. It can be synthesized by heating succinic anhydride with hydroxylamine or hydroxylamine hydrochloride .

  3. Leaving group - Wikipedia

    en.wikipedia.org/wiki/Leaving_group

    In this usage, a leaving group is a less formal but more commonly used synonym of the term nucleofuge. In this context, leaving groups are generally anions or neutral species, departing from neutral or cationic substrates, respectively, though in rare cases, cations leaving from a dicationic substrate are also known. [3]

  4. Nucleophilic substitution - Wikipedia

    en.wikipedia.org/wiki/Nucleophilic_substitution

    This means that the better the leaving group, the faster the reaction rate. A general rule for what makes a good leaving group is the weaker the conjugate base, the better the leaving group. In this case, halogens are going to be the best leaving groups, while compounds such as amines, hydrogen, and alkanes are going to be quite poor leaving ...

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  8. Desulfonylation reactions - Wikipedia

    en.wikipedia.org/wiki/Desulfonylation_reactions

    Sulfones with a good leaving group in the β position may undergo reductive elimination under desulfonylation conditions to afford alkenes. This process is a key step of the Julia olefination , which yields alkenes via addition of an α-sulfonyl carbanion to an aldehyde followed by reductive elimination.

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