Hello. I'm sorry if this is the wrong forum. I opted to post in the Biological Chemistry section, but this question is more to do with synthesis and internal reactions, so I thought I'd put it here.
I'm having some trouble with a particular part of my course. Basically, we're usually given a couple of precursors, and we have to determine disconnections in a given polyketide. Some questions are quite straight forward, especially when it's easy to spot a stray methyl group or something. But the questions are a little harder when there are no obvious indications of where the primer group is located.
If you're confused about what I mean, check out the file I attached. The top reaction shows how Malonyl/Acetyl CoA derivative reacts with itself to form a polyketide, and the second shows what we're expected to be able to deduce from any given polyketide. The colours represent the carbons from the original reactants before they became a chain. The bottom examples are questions where I am unsure of how to determine such disconnections.
Basically, I am unsure of how to properly utilise the information given to me in those boxes.
Any help would be appreciated. I don't expect you to show me how to do all 3 (though that'd be awesome). I really just want to understand the logic in working backwards from any given polyketide. 1 would be enough. I understand the forward reaction, but going backwards really has me stumped.
Thank you.