L-Selectride Reduction Mechanism | Organic Chemistry @OrganicMechanismsChannel

Uploaded September 2021 | Updated September 2026, 1 week ago

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

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

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L-Selectride Reduction Mechanism | Organic Chemistry