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Topic: Julia or Schlosser Mod. for E alkenes?  (Read 2178 times)

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Offline subro

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Julia or Schlosser Mod. for E alkenes?
« on: May 16, 2015, 03:01:55 PM »
Hello, I have a question about which is the best way for synthesize an stereoselectively E alkene. The two options that I'm comparing are Julia olefination (well, Kociensky mod. because it's simpler) or Schlosser Mod. (Wittig with lithium salts). I dont know with which way I will have more stereoselectivity.

Any idea?

Thanks in advance.

Offline pgk

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Re: Julia or Schlosser Mod. for E alkenes?
« Reply #1 on: May 18, 2015, 02:24:38 PM »
Try the stereoselective Witting. Might be a lower yield but the base preparation, overall operation and purification are simple. However, the stereoselectivity of the Witting reaction depends on the stucture of the Witting reagent (See the literature).

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