Yes, I have some knowledge about it. Retrosynthetic analysis is done by going from the final product to smaller and cheaper starting materials. Synthons, functional group interconversions and cleavages play a crucial role.
You may want to view http://www.cmbi.ru.nl/cheminf/ira/strat.shtml for a good explanation.
Tell me an example, and I'll try to solve it for you.
It's common sense. I would suggest that you first attempt complex synthetic problems themselves, perhaps the retrosynthetic idea will make sense to you afterwards.
Of course, suf7, please try these first in light of the information I gave you, and if you're stuck, call for help. GCT, thanks to you about reminding this.
A great text on learning the logic of retrosynthetic analysis is Designing Organic Synthesis by Stuart Warren (Wiley, 1978). It's set up like a workbook and helps you to learn and understand retrosynthetic disconnections.
i am a final year student and am having problems in getting to grips with some problems that i have been set for an assignment, and was wondering if anyone culd help me with them?
Organic chemistry is my weakness, hence the plea for help?
would anyone be willing to have a look at the problems and possibly help me?