Uploaded July 2021 | Updated September 2026, 1 week ago
The mechanism for a Noyori Asymmetric Hydrogenation in which a ketone is enantioselectivity reduced to the corresponding alcohol. Depending on the catalyst used, the resulting alcohol can be selectively produced in ether the R or S form. In the mechanism shown, the R form or the catalyst is used and therefore the R form of the corresponding alcohol is produced. I the S form or the catalyst was used, then the S form of the alcohol would be produced.
Music: Walkout – YouTube Audio Library
The mechanism for a Noyori Asymmetric Hydrogenation in which a ketone is enantioselectivity reduced to the corresponding alcohol. Depending on the catalyst used, the resulting alcohol can be selectively produced in ether the R or S form. In the mechanism shown, the R form or the catalyst is used and therefore the R form of the corresponding alcohol is produced. I the S form or the catalyst was used, then the S form of the alcohol would be produced.
Music: Walkout – YouTube Audio Library










