Total synthesis of alpha-cedrene: A new strategy utilizing N-aziridinylimine radical chemistry

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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
DOI
10.1016/S0040-4039(98)01680-3
URI
http://hdl.handle.net/10203/75373
Appears in Collection
CH-Journal Papers(저널논문)
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