User:Tkadm30/Notebook/Drospirenone: Difference between revisions
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* [[Pyrrolidines]] | * [[Pyrrolidines]] | ||
* [http://en.wikipedia.org/wiki/Beckmann_rearrangement | * [http://en.wikipedia.org/wiki/Beckmann_rearrangement#Cyanuric_chloride_assisted_Beckmann_reaction Cyanuric chloride assisted Beckmann reaction] | ||
Revision as of 07:12, 15 June 2013
- CYP450 mediated [1] (A spironolactone derived alkyloid)
- optical isomerism (C2) : a HSL (homoserine) lactone derivative ?
- A high risks of hyperkalemia (K+) was found with long-term use of Yasmin. [2]
- Ethics of birth control with chiral Schiff base alkaloids in orthogonal Fmoc-carbonyl nucleophilic catalysis? See Grignard reagent .
Yb(OTf)3-catalyzed synthetic pyrrolidines via aldimine-protected analogs (Drosperinone)
- Hence, is there a Yb(OTf)3 (diastereoselective) route to remote activation of Fmoc-protected alkaloids via MW catalysis of C(2)-symmetric amines, ie Drospirenone ? [3, 4]
References
- http://en.wikipedia.org/wiki/Drospirenone
- http://en.wikipedia.org/wiki/Spironolactone
- Diastereoselective Synthesis of Pyrrolidines via the Yb(OTf)3 Catalyzed Three-Component Reaction of Aldehydes, Amines, and 1,1-Cyclopropanediesters
- http://en.wikipedia.org/wiki/Ketoxime
- http://en.wikipedia.org/wiki/Aldimine
