Reactions of Grignard Reagents
Here’s the summary for today’s post: So far in this series we’ve introduced organometallic compounds and said that their carbons tend to be nucleophilic. We’ve
Read moreHere’s the summary for today’s post: So far in this series we’ve introduced organometallic compounds and said that their carbons tend to be nucleophilic. We’ve
Read moreOpening of epoxides with base a summary of what we talk about today: In the last post we discussed the reactions of epoxides under acidic
Read moreHere’s what we’re covering in this post. Opening Epoxides With Aqueous Acid In the last post, we saw some examples of how epoxides are considerably
Read moreIn a blatant plug for the Reagent Guide and the Reagents App for iPhone, each Friday I profile a different reagent that is commonly encountered in Org 1/ Org
Read moreIn a blatant plug for the Reagent Guide, each Friday I profile a different reagent that is commonly encountered in Org 1/ Org 2. mCPBA (meta-chloroperoxybenzoic
Read moreLast time we talked about how some interesting electronic effects can lead to unexpected results in organic chemistry. Today we look at three examples of
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