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| Hello everyone I am a second semester organic chemistry student. My class focuses a lot on organic synthetic pathways. Most of our synthesis reactions are 5-8 steps. I've read in our book a little bit about retrosynthesis, in order to help improve working out the problems, but I was just curious if you guys had any suggestions to offer on little key points to notice that make connecting the reactiosn much easier. Thanks GreenEggsNSpam -- Paul J. Franklin(moderator - sci.chem.organic.synthesis) [Only registered users see links. ] Georgia State University <[Only registered users see links. ].edu> Atlanta, GA |
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