Chemical Forums
Chemistry Forums for Students => Organic Chemistry Forum => Organic Chemistry Forum for Graduate Students and Professionals => Topic started by: Dan on November 09, 2012, 12:23:34 PM
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Explain the following reaction sequence, predicting the structure of compound 2.
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The first step is a bromolactonization with the carboxylic acid on the right. The remaining -COOH on the left is then converted to a mixed anhydride and reduced with sodium borohydride to the alcohol. Finally the resultant alcohol is BOM protected with BOMCl.
2 is then taken forward. The Zn inserts into the C-Br bond to do an elimination, kicking out -COO- and reforming the alkene. The next step with the azide material is a bit odd to me. It looks like some weird Staudinger variant but I don't know how we get rid of the carbon from the -COOH and replace it with a nitrogen.
The osmium tetroxide oxidized the olefin to the aldehyde which is then reduced to the alcohol.
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Good so far. Almost there.
There is a typo, I apologise, it is diphenylphosphoryl azide (PhO)2P(O)N3 (not Ph2P(O)N3). It has now been corrected in my original post.
I will give a hint in a couple of days if nobody else comes forward.
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Ahh, I've been away from organic chemistry for too long. I would have gotten this quicker two years ago.
The third to last step (step E) is a Curtius rearrangement. Once I drew out the BOC group and realized we had tert-butanol in the mix I finally saw it.
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Yes indeed, nicely done.
I will post the full solution when I get time, probably tomorrow, unless you fancy putting your words into pictures?
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I may draw it out tonight. The wife takes the TV on Mondays and Tuesdays to watch Dancing with the Stars :P
Although I do miss out on Monday night football, the advantage is that I get some quite time to browse the forums and do some reading :)
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Hi,
do you have a reference for the the problem,
my group does literature reviews and mechanisms, and would like to have it as a mechanism problem for the group.
PS. nicely done Stewie
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I have attached the solution (but not with full mechanism).
Taken from Terashima's synthesis of (+)-FR900482
The steps from this problem come from:
Tet. Lett. 1996, 37, 3475 Link (http://www.sciencedirect.com/science/article/pii/0040403996005941)
The rest of the synthesis continues:
Tet. Lett. 1996, 37, 3479 Link (http://www.sciencedirect.com/science/article/pii/0040403996005953)
The endgame is described in more detail here:
Tet. Lett. 1996, 37, 3471 Link (http://www.sciencedirect.com/science/article/pii/004040399600593X)