
Hydroxy-Substituted Trialkyloxonium Alkoxide - O+ on one side, O- on the other side, but doesn't self-destruct
Just synthesized by Otsuki et. al., and summarized in Chemical & Engineering News article:

Just synthesized by Otsuki et. al., and summarized in Chemical & Engineering News article:
I created this article recently, taking the liberty to name this reaction after its discoverer.
I'll just leave it to y'all to appreciate.
Can someone please tell me why there are little clear sand type pebbles in my meth. And it's not just in the powder. It could literally be a full solid shard and once it melts I have these clear little pebbles in my bubble
12 step synthesis with a 0.4% yeild. The stereochemistry of the phosphorus depends on the stereochemistry of the glycerol. Its called pseudo asymmetry. I cried for 20 mintues when I got the LCMS
Since CH5+ gets brought up a lot here, I thought Id share this blurb in Modern Physical Organic Chemistry (Anslyn & Dougherty)
CH5+ may not have "bonds" at all, so no bonding rules are violated! Instead it's just a completely delocalized, quantum mechanical cloud of protons and electrons around carbon. Much better :)
Apparently quadruple bonds are a thing (the bond is proposed to be made from the overlap of 4 d orbitals of the chromium)
The thing also polyimerises, which is neat