Uploaded February 2022 | Updated September 2026, 2 weeks ago
The mechanism for a Hoch-Campbell aziridine synthesis. The Hoch-Campbell aziridine synthesis entails treatment of ketoximes with excess Grignard reagents and subsequent hydrolysis of the organometallic complex.
Music: Phasing – Mokka
The mechanism for a Hoch-Campbell aziridine synthesis. The Hoch-Campbell aziridine synthesis entails treatment of ketoximes with excess Grignard reagents and subsequent hydrolysis of the organometallic complex.
Music: Phasing – Mokka

![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)








![N-Selectride Reduction Mechanism | Organic Chemistry
The mechanism for the reduction of a ketone to an alcohol using N-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: Abstract Wall – Infraction N-Selectride Reduction Mechanism | Organic Chemistry](https://i.ytimg.com/vi/sTgbTyXcB2s/mqdefault.jpg)