Figure 1: Synthetic strategies to access secondary and tertiary alcohols by carbonyl addition reactions. Despite considerable advances, and the abundance of organometallic reagents developed for ...
Carbonyl‐olefin metathesis reactions have emerged as an invaluable strategy for the direct formation of carbon–carbon bonds, enabling the efficient construction of complex molecular architectures.
Carbonyls (C=O groups) are popular reactive handles. But carbonylation reactions, which create these useful groups by appending carbon monoxide to aryl halides or alkyl halides with the help of a ...
Emory University researchers led by Kyle Biegasiewicz have repurposed enzymes to produce diazo compounds from hydrazones ...
This module covers aldehydes and ketones as the substrates and products of redox reactions. Structure is explained with both Lewis structures and molecular orbitals to discuss mechanisms in the ...
Penn State researchers have uncovered a surprising twist in a foundational chemical reaction known as oxidative addition. Typically believed to involve transition metals donating electrons to organic ...
Halogen bonds were first proposed as an activating interaction in 2008, but this alternative type of organocatalysis was ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results