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Access to 6a-Alkyl Aporphines: Synthesis of (±)-N-Methylguattescidine
- Source :
- The Journal of Organic Chemistry. 81:10062-10070
- Publication Year :
- 2016
- Publisher :
- American Chemical Society (ACS), 2016.
-
Abstract
- (-)-N-Methylguattescidine (3) is an alkaloid recently isolated from Fissistigma latifolium and assigned as a rare example of a 6a-alkyl aporphine. Herein, we report the synthesis of (±)-3 and the des-hydroxyl derivative 4 using our previously reported ortho-phenol arylation methodology mediated by the XPhos precatalyst as a key synthetic step. In addition, substituents on the aryl halide portion of the ortho-phenol arylation substrates significantly influenced the formation of an oxidized side product.
- Subjects :
- chemistry.chemical_classification
Aporphines
biology
010405 organic chemistry
Stereochemistry
Proton Magnetic Resonance Spectroscopy
organic chemicals
Aryl halide
Organic Chemistry
Stereoisomerism
Fissistigma
biology.organism_classification
01 natural sciences
Mass Spectrometry
0104 chemical sciences
010404 medicinal & biomolecular chemistry
chemistry.chemical_compound
chemistry
XPhos
Aporphine
Carbon-13 Magnetic Resonance Spectroscopy
Derivative (chemistry)
Alkyl
Subjects
Details
- ISSN :
- 15206904 and 00223263
- Volume :
- 81
- Database :
- OpenAIRE
- Journal :
- The Journal of Organic Chemistry
- Accession number :
- edsair.doi.dedup.....fc3486681fc21d398237588384b2bc92
- Full Text :
- https://doi.org/10.1021/acs.joc.6b02024