A tandem radical cyclization route to tricyclo[4.3.n.0(1,5)]alkanes
A facile route to tricyclo[4.3.n.0(1.5)]alkane skeletons from conjugated cyclic enones was developed through tandem free radical cyclization reaction sequence involving the cyclopropylmethyl radical mediated rearrangement. The scope and limitation of the reaction was investigated. (C) 2004 Elsevier Ltd. All rights reserved.
- Publisher
- PERGAMON-ELSEVIER SCIENCE LTD
- Issue Date
- 2004-09
- Language
- English
- Article Type
- Article
- Keywords
REARRANGEMENT; CONSTRUCTION; SKELETON
- Citation
TETRAHEDRON LETTERS, v.45, no.39, pp.7225 - 7229
- ISSN
- 0040-4039
- Appears in Collection
- CH-Journal Papers(저널논문)
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