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12 Nov 2019
Heck-Mizoroki, Sonagashira, and Suzuki-Miyaura question. All data provided. It wants three different synthesis one HM, one Sonagashira and one SM. You can make whichever one whichever way you want it just has to be made with one of those three syntheses using a conjugated diene and one single cross coupling reaction
3. Make the three molecules below using all three Ch. 21 cross-coupling reactions Hecok- Mizoroki, Suzuki-Mi reactants, you may use any alkyl monobromide (no other FG's) with six or fewer ca NOT use Grignard chemistry to make the new C-C bond! Retrosynthesis w promise!! Specifically, each product is made from a conjugated diene in a sing the diene which would be use to make it. For each C-C bond formation reaction, write the name of it a reaction conditions. (21 points) yaura, and Sonogashira - a different one for each molecule). As the ll help you plan-1 le reaction. Draw required to make each product, then choose which type of coupling to longside the OH OH Br Br
Heck-Mizoroki, Sonagashira, and Suzuki-Miyaura question. All data provided. It wants three different synthesis one HM, one Sonagashira and one SM. You can make whichever one whichever way you want it just has to be made with one of those three syntheses using a conjugated diene and one single cross coupling reaction
3. Make the three molecules below using all three Ch. 21 cross-coupling reactions Hecok- Mizoroki, Suzuki-Mi reactants, you may use any alkyl monobromide (no other FG's) with six or fewer ca NOT use Grignard chemistry to make the new C-C bond! Retrosynthesis w promise!! Specifically, each product is made from a conjugated diene in a sing the diene which would be use to make it. For each C-C bond formation reaction, write the name of it a reaction conditions. (21 points) yaura, and Sonogashira - a different one for each molecule). As the ll help you plan-1 le reaction. Draw required to make each product, then choose which type of coupling to longside the OH OH Br Br