Total synthesis of alpha-cedrene: A new strategy utilizing N-aziridinylimine radical chemistry
Tandem free radical cycloaddition reaction of the N-Aziridinylimine intermediate produced tricyclo[5.3.1.0(1,5)]undecane skeleton stereoselectively. A total synthesis of alpha-cedrene was completed in three step sequence from the cyclization product, (C) 1998 Elsevier Science Ltd. All rights reserved.
- Publisher
- PERGAMON-ELSEVIER SCIENCE LTD
- Issue Date
- 1998-10
- Language
- English
- Article Type
- Article
- Keywords
CARBONYL-COMPOUNDS; ORGANIC-SYNTHESIS; CYCLIZATION; REAGENT; IMINES
- Citation
TETRAHEDRON LETTERS, v.39, no.42, pp.7713 - 7716
- ISSN
- 0040-4039
- Appears in Collection
- CH-Journal Papers(저널논문)
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