- A conjugated diene in an s-cis conformation reacts with
- A dienophile to form
- A 6-membered ring with one double bond
My Little s-Cis Diene (Diels- Alder Reaction Animated)
We know that this reaction can occur in the lab, but can it happen naturally?
The answer is yes. A photosynthetic fungus, Macrophoma commelinae, synthesizes the compound macrophomate synthase in complex with pyruvate through a three step proccess, the second of the reactions in this process is a diels alder reaction. The entire reaction process is illustrated below:
The diene of this reaction is known as 2-pyrone (IUPAC: pyran-2-one) and is illustrated below:
The dienophile of this reaction is ethyl propiolate (IUPAC: Ethyl acetylenecarboxylate) and is illustrated below:
The reaction conditions of this process also include that the reaction occurs entirely within the fungus itself, and must be catalyzed by the enzyme MPS.
Sources (In order of appearance):
Video:
Ethyl propriolate: ethyl propiolate. Pub Chem Compound. http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=12182#itabs-2d (accessed Feb 03, 2014)