A facile construction of the quadranoid skeleton: Application to the total synthesis of (+/-)-suberosenone
A tandem free radical cyclization-rearrangement sequence was designed and executed to produce tricyclo[4.3.2.0(1,5)]undecane 7 from cyclopentene 6A in a single operation. The total synthesis of suberosenone was accomplished from 7.
- Publisher
- AMER CHEMICAL SOC
- Issue Date
- 2000-06
- Language
- English
- Article Type
- Article
- Keywords
ORGANOSELENIUM CHEMISTRY; ORGANIC-SYNTHESIS; QUADRONE; KETONES; REARRANGEMENT; SUBEROSENONE; RADICALS; ALCOHOLS
- Citation
ORGANIC LETTERS, v.2, no.13, pp.1951 - 1953
- ISSN
- 1523-7060
- Appears in Collection
- CH-Journal Papers(저널논문)
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