| Weight | 223.272 g/mol |
|---|---|
| Formula | C12H17NO3 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
Calycotomine (4356-47-2)
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- Enantioselective synthesis of (S)-calycotomine employing catalytic asymmetric hydrogenation with an iridium(I)(R)-BINAPphthalimide complex (Tetrahedron-asymmetry, 1998)
- Continuous-flow enzymatic resolution strategy for the acylation of amino alcohols with a remote stereogenic centre: Synthesis of calycotomine enantiomers (Tetrahedron-asymmetry, 2013)
- Cyclization of Some O-Substituted Derivatives of N-(3,4-Dimethoxy--phenylethyl)glycolamide; Synthesis of ()-Calycotomine (Journal of Organic Chemistry, 1961)
- Reissert compound studies. VII. The synthesis of calycotomine (Journal of Heterocyclic Chemistry, 1964)
- Extension of the Bobbitt Acetal Cyclization to the Elaboration of 1-Hydroxymethyl-Substituted Simple Tetrahydroisoquinolines. A New Synthesis of Calycotomine (Synthetic Communications, 1993)
- The synthesis of the isoquinoline alkaloid calycotomine via functionalization of enamide double bonds (Heterocycles, 1987)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCOC1=C(C=C2C(NCCC2=C1)CO)OC
-
InChIKeyJVLGDDNDVOSMSI-UHFFFAOYSA-N
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Calycotomine
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