Highly enantioselective cascade synthesis of spiropyrazolones
✍ Scribed by Zea, Alex; Alba, Andrea-Nekane R.; Mazzanti, Andrea; Moyano, Albert; Rios, Ramon
- Book ID
- 120081607
- Publisher
- Royal Society of Chemistry
- Year
- 2011
- Tongue
- English
- Weight
- 255 KB
- Volume
- 9
- Category
- Article
- ISSN
- 1477-0520
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## Abstract The synthesis of spiro compounds through a Michael–Michael–aldol reaction is reported. The reaction affords spiropyrazolone derivatives in good yields, in almost diastereo‐ and enantiopure form, and is catalyzed by diphenylprolinol derivatives. The reaction showed strong nonlinear effec
## Abstract The title compounds are obtained through a Michael—Michael‐aldol reaction in good yields and with high diastereo‐ and enantioselectivity.
Highly Enantioselective Organocatalytic Cascade Reaction for the Synthesis of Piperidines and Oxazolidines. -Organocatalyzed Michael addition of amidomalonates, e.g. (I) and (VI), towards enals (II) followed by intramolecular hemiaminal formation provides enantioenriched piperidine derivatives (III)