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A selective C–H insertion/olefination protocol for the synthesis of α-methylene-γ-butyrolactone natural products
- Source :
- Organic & Biomolecular Chemistry. 14:1641-1645
- Publication Year :
- 2016
- Publisher :
- Royal Society of Chemistry (RSC), 2016.
-
Abstract
- A regio- and stereoselective one-pot C-H insertion/olefination protocol has been developed for the late stage installation of α-methylene-γ-butyrolactones into conformationally restricted cyclohexanol-derivatives. The method has been successfully applied in the total synthesis of eudesmanolide natural product frameworks, including α-cyclocostunolide.
- Subjects :
- Biological Products
Natural product
Molecular Structure
010405 organic chemistry
Stereochemistry
Organic Chemistry
Late stage
α methylene γ butyrolactone
Total synthesis
Stereoisomerism
010402 general chemistry
01 natural sciences
Biochemistry
0104 chemical sciences
chemistry.chemical_compound
4-Butyrolactone
chemistry
Stereoselectivity
Physical and Theoretical Chemistry
Subjects
Details
- ISSN :
- 14770539 and 14770520
- Volume :
- 14
- Database :
- OpenAIRE
- Journal :
- Organic & Biomolecular Chemistry
- Accession number :
- edsair.doi.dedup.....d253c5f0ff91413c98766f4b282870ac
- Full Text :
- https://doi.org/10.1039/c5ob02579f