(8α,9S)-9-aMino-Cinchonan-6'-ol
(8α,9S)-9-aMino-Cinchonan-6'-ol Basic information
- Product Name:
- (8α,9S)-9-aMino-Cinchonan-6'-ol
- Synonyms:
-
- (8α,9S)-9-aMino-Cinchonan-6'-ol
- (8α, 9S)-(+)-9-AMino-cinchonan-6'-ol, Min. 90%
- (8Α,9S)-(+)-9-AMINO-CINCHONAN-6'-OL,MIN.90%
- 9S)-(+)-9-Amino-cinchonan-6'-ol, min. 90%
- 9-amino-(9-deoxy)epi-6-hydroxycinchonidine
- Cinchonan-6'-ol, 9-amino-, (8α,9S)-
- 4-((S)-Amino((1S,2S,4S,5R)-5-vinylquinuclidin-2-yl)methyl)quinolin-6-ol
- (8α,9S)-9-amino-Cinchonan-6'-ol
- CAS:
- 960050-59-3
- MF:
- C19H23N3O
- MW:
- 309.41
- Mol File:
- 960050-59-3.mol
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(8α,9S)-9-aMino-Cinchonan-6'-ol Chemical Properties
- alpha
- +107.9° (c 1.0, CHCl3)
- Boiling point:
- 501.7±45.0 °C(Predicted)
- Density
- 1.24±0.1 g/cm3(Predicted)
- pka
- 8.92±0.40(Predicted)
- form
- Powder
- color
- off-white to pale brown
- Stability:
- store cold
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(8α,9S)-9-aMino-Cinchonan-6'-ol Usage And Synthesis
Reaction
1. [2+3]-dipolar cycloaddition of cyclic enones.
2. Activation of α,β-unsaturated carbonyl compounds:
a) vinylogous α-ketol rearrangement.
b) vinylogous Michael addition of β-substituted α,β-unsaturated cyclohexanones.
3. Michael addition
a) α-nitroacetate to α,β-unsaturated ketones.
b) Diastereodivergent Michael addition to α-substituted, α,β-unsaturated ketones.
4. α-benzoyloxylation of α-branched aldehydes.
5. [4+2]-cycloadditions of β-substituted α,β-unsaturated cyclohexanones with polyconjugated malonitriles.
6. Vinylogous organocascade catalysis with control of remote stereochemistry in the synthesis of spirocyclic oxindoles.
(8α,9S)-9-aMino-Cinchonan-6'-olSupplier
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