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A Novel Synthesis of Functionalized Allylsilanes
- Source :
- Organic Letters. 6:1849-1852
- Publication Year :
- 2004
- Publisher :
- American Chemical Society (ACS), 2004.
-
Abstract
- A novel facile synthesis of substituted and functionalized allylsilane has been developed. This essentially one-pot procedure involves (1) (dimethylphenylsilyl)methyl cerium chloride addition to cyclopropyl ketone and (2) MgI(2) etherate-mediated Julia homoallylic transposition of the corresponding cyclopropyl carbinol. The bifunctional homoiodo allylsilanes, readily accessible by this method, would be useful and versatile synthons in organic synthesis. [reaction: see text]
- Subjects :
- chemistry.chemical_classification
Ketone
Organic Chemistry
Synthon
chemistry.chemical_element
General Medicine
Combinatorial chemistry
Biochemistry
Chloride
Transposition (music)
chemistry.chemical_compound
Cerium
chemistry
medicine
Organic chemistry
Organic synthesis
Physical and Theoretical Chemistry
Bifunctional
medicine.drug
Subjects
Details
- ISSN :
- 15237052 and 15237060
- Volume :
- 6
- Database :
- OpenAIRE
- Journal :
- Organic Letters
- Accession number :
- edsair.doi.dedup.....d638732b9f7b5510fa06e90aa76622cc
- Full Text :
- https://doi.org/10.1021/ol049311v