| Version | Summary | Created by | Modification | Content Size | Created at | Operation |
|---|---|---|---|---|---|---|
| 1 | Helena Kang | -- | 137 | 2026-10-29 09:10:21 | | | |
| 2 | Catherine Yang | -14 word(s) | 123 | 2026-10-29 09:26:59 | | |
Alkylation chemistry comprises reactions that form a bond between an alkyl fragment and a nucleophilic atom or carbon centre. In its classical organic-chemical sense, an electron-rich substrate displaces a leaving group from, or otherwise reacts with, an alkylating agent; the outcome is governed by the structures and electronic properties of both partners and by the reaction mechanism. The term therefore encompasses carbon alkylation as well as N-, O-, S-, and related heteroatom alkylations. Alkylation is distinguished from arylation by transfer of an alkyl, rather than an aryl, group, and its mechanistic description commonly involves polar substitution or addition pathways [1]. O-Alkylation is a defined subclass in which an oxygen nucleophile becomes bonded to the transferred alkyl group [2].