Talk:Ether: Difference between revisions
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→Synthesis of Chromenone from Chalcone(Nannan Ji): new section |
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The formation of 1-methoxy-1-methylcyclohexane first by oxymercuration, then the alcohol attack and break the three-membered ring on the more saturated C, and finally the borohydride substitute the mercury. | The formation of 1-methoxy-1-methylcyclohexane first by oxymercuration, then the alcohol attack and break the three-membered ring on the more saturated C, and finally the borohydride substitute the mercury. | ||
== Synthesis of Chromenone from Chalcone(Nannan Ji) == | |||
[[File:Chromenone_synthesis.png]] | |||
Revision as of 14:38, 7 May 2018
Trityl ether (Grace Park)
2-methoxybutane (Bretta McCall)
Alkene to Ether: Formation of 2-methoxy-2-methylbutane (Yuwei Pan)
File:2-methoxy-2-methylbutane.png
1-methoxy-1-methylcyclohexane by oxymercuration (Kelsey Zhang)
The formation of 1-methoxy-1-methylcyclohexane first by oxymercuration, then the alcohol attack and break the three-membered ring on the more saturated C, and finally the borohydride substitute the mercury.