A Cascade Cyclization Route to Adjacent Bistetrahydrofurans from Chiral Triepoxyfarnesyl Bromides
A number of isomeric bistetrahydrofuran analogues were prepared from triepoxy farnesyl bromides by a zinc-initiated reduction−elimination and in situ Lewis acid-promoted cascade cyclization.
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| Veröffentlicht in: | Journal of organic chemistry 2008-09, Vol.73 (17), p.6753-6757 |
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| container_end_page | 6757 |
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| container_issue | 17 |
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| container_title | Journal of organic chemistry |
| container_volume | 73 |
| creator | Marshall, James A Hann, Ronald K |
| description | A number of isomeric bistetrahydrofuran analogues were prepared from triepoxy farnesyl bromides by a zinc-initiated reduction−elimination and in situ Lewis acid-promoted cascade cyclization. |
| doi_str_mv | 10.1021/jo801188w |
| format | Article |
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| ispartof | Journal of organic chemistry, 2008-09, Vol.73 (17), p.6753-6757 |
| issn | 0022-3263 1520-6904 |
| language | eng |
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| source | ACS Publications; MEDLINE |
| subjects | Catalysis Chemistry Cyclization Epoxy Compounds - chemistry Exact sciences and technology Furans - chemical synthesis Heterocyclic compounds Heterocyclic compounds with o, s, se, te hetero atom and condensed derivatives Hydrocarbons, Brominated - chemistry Models, Chemical Organic chemistry Oxidation-Reduction Prenylation Preparations and properties Spectrum Analysis Stereoisomerism Zinc - chemistry |
| title | A Cascade Cyclization Route to Adjacent Bistetrahydrofurans from Chiral Triepoxyfarnesyl Bromides |
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