textjournal article
Synthesis of the Lycopodium Alkaloid (+)-Lycoflexine
Abstract
The first total synthesis of (+)-lycoflexine (1), a constituent of Lycopodium clavatum var. inflexum, has been accomplished in eight steps with 13% overall yield. Our synthesis covers four one-pot reactions, including a tandem Sakurai/aldol sequence, a novel hydroboration/oxidation procedure, a deprotection/transannular Mannich reaction, and as a highlight, a tandem catalysis cascade combining an enynene ring-closing metathesis and a selective hydrogenation- Text
- Journal contribution
- Biophysics
- Biochemistry
- Microbiology
- Genetics
- Molecular Biology
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- Evolutionary Biology
- Infectious Diseases
- Chemical Sciences not elsewhere classified
- metathesi
- Sakurai
- inflexum
- sequence
- Mannich
- hydrogenation
- synthesis
- enynene
- deprotection
- hydroboration
- constituent
- tandem catalysis cascade
- LycoflexineThe
- Alkaloid
- Synthesi
- Lycopodium clavatum var
- procedure
- lycoflexine