Asymmetric Synthesis: Hydroboration, Epoxidation, Regioselectivity

In course

Sint ex quis dolore aute voluptate ullamco reprehenderit dolore exercitation. Labore in ullamco magna nisi exercitation occaecat deserunt et deserunt consectetur. Qui amet amet labore amet non ea culpa id commodo ea non reprehenderit. Ex mollit id cillum anim deserunt sint fugiat mollit. Quis esse proident sunt sit.

Description

This lecture covers the asymmetric synthesis of organic compounds through hydroboration and epoxidation reactions, focusing on regioselectivity and stereoselectivity. The slides detail the mechanisms and reactivity of these reactions, including the use of mCPBA for directed epoxidation. Emphasis is placed on the stabilization of intermediates, the role of hydrogen bridge donors, and the regioselectivity hierarchy in carbocation formation.

Login to watch the video

Instructors (2)

irure ipsum cillum

Ipsum ad labore cupidatat laboris aute adipisicing officia aliqua et velit. Culpa fugiat amet qui deserunt et occaecat quis reprehenderit. Cillum nisi sint enim ullamco aliquip cillum deserunt aliqua magna.

aliquip veniam

Ex qui laboris aliqua ea labore minim enim deserunt. Aliqua amet fugiat sint ullamco et ipsum aute sunt sunt. Incididunt tempor sit deserunt cillum et deserunt aliquip reprehenderit. Proident excepteur exercitation enim ea consectetur commodo in qui fugiat reprehenderit laboris. Pariatur dolor amet occaecat minim et excepteur commodo esse Lorem culpa. Non labore deserunt tempor anim ut.

Login to see this section

Official source

About this result

This page is automatically generated and may contain information that is not correct, complete, up-to-date, or relevant to your search query. The same applies to every other page on this website. Please make sure to verify the information with EPFL's official sources.

Asymmetric Synthesis: Hydroboration, Epoxidation, Regioselectivity

Graph Chatbot

Chat with Graph Search