Uploaded November 2021 | Updated September 2026, 1 week ago
The mechanism for the addition of a 2-Methoxyethoxymethyl ether (MEM) protecting group which is used in organic synthesis as a protecting group for alcohols. In addition to other deprotection methods, a highly selective cleavage method has been developed using cerium(III) chloride.
Music: Alone – Infraction
The mechanism for the addition of a 2-Methoxyethoxymethyl ether (MEM) protecting group which is used in organic synthesis as a protecting group for alcohols. In addition to other deprotection methods, a highly selective cleavage method has been developed using cerium(III) chloride.
Music: Alone – Infraction










![L-Selectride Reduction Mechanism | Organic Chemistry
The mechanism for the reduction of a ketone to an alcohol using L-Selectride. There are multiple reagents that have the formula M[HB(sec-Bu)3] which are all used as reducing agents. There are three different cations with these reducing agents and they are L-Selectride (lithium), N-Selectride (sodium), and K-Selectride (potassium). Due to the sec butyl groups on these reducing agents, these reagents are sensitive to steric influences which has the potential to allow for stereoselective reactions.
Music: Gray Clouds – Infraction L-Selectride Reduction Mechanism | Organic Chemistry](https://i.ytimg.com/vi/oEoTzkAP0ak/mqdefault.jpg)