
Cyclohexanone is readily available Compound which then undergoes Wittig reaction to give alkene. Then epoxidation by mCPBA.
Ring opening of unsymmetrical epoxide in basic medium occurs at less substitude side followed by protonation complete the synthesis.
OH NH2 6. Syntheisze the following Retrosynthetic Analysis Synthesis
4. (3 pts) Using retrosynthetic analysis, provide a synthesis for the following molecule. Place the required reagents next to the arrows and the necessary intermediate in the box provided. Me NH но HK он 1 4 5. 6. 3. 2. NH2 O) 08
4. (3 pts) Using retrosynthetic analysis, provide a synthesis for the following molecule. Place the required reagents next to the arrows and the necessary intermediate in the box provided. Me NH но HK он 1 4 5....
Using retrosynthetic analysis,
provide a synthesis for the following molecule. Place the required
reagents next to the arrows and the necessary
HH iPr: + MeOCCO Me 1. 8. 2. 9. 3. 7. 4. 5. Me NH2 6. Me MeOCCO Me
4. (3 pts) Using retrosynthetic analysis, provide a synthesis for the following molecule. Place the required reagents next to the arrows and the necessary intermediate in the box provided. HH iPr Meo, co Me co, 8. 2. 3. 7. 5. Me NH2 Me MeOCCO Me 6.
4. (3 pts) Using retrosynthetic analysis, provide a synthesis for the following molecule. Place the required reagents next to the arrows and the necessary intermediate in the box provided. Η. Η Me MeOCCO,Me 1. 8. 2. 9 3 7. 4. 5 NH2 6 MeOCCO Me
4. (3 pts) Using retrosynthetic analysis, provide a synthesis for the following molecule. Place the required reagents next to the arrows and the necessary intermediate in the box provided. Η Η N iPr MeO2C CO Me co 1. 8. 2. 9. 3. 7. 4. 5. Me NH2 6. Me MeOCCO Me
ОН Syntheisze the following alcohol Retrosynthetic Analysis Synthesis
5. Syntheisze the following alcohol ~ Retrosynthetic Analysis Synthesis
1. Synthesize the following ester Retrosynthetic Analysis Synthesis
4.Synthesize the following sulfide ci Retrosynthetic Analysis Synthesis
2. Synthesize the following amide ci' Retrosynthetic Analysis Synthesis