Anionic Cyclization of N-(trans-2,3-Diphenylaziridin-1-yl)imines: Its Application to Sesquiterpene Synthesis via Consecutive Carbon-Carbon Bond-Formation Approach
The anionic consecutive carbon-carbon (CC-C) bond formation can be achieved by the anionic cyclizations of N-(trans-2,3-diphenylaziridin-1-yl)imines with alkyllithiums. The synthetic efficiency of CC-C bond-formation approach has been demonstrated in the synthesis of dl-pentalenene and dl-cedrone.
- Publisher
- Georg Thieme Verlag Kg
- Issue Date
- 2010-06
- Language
- English
- Article Type
- Article
- Keywords
N-AZIRIDINYL IMINES; TANDEM RADICAL CYCLIZATION; EFFICIENT SYNTHESIS; BETA-CEDRENE; ROUTE; ALKYLLITHIUMS; PENTALENENE; STEREOCHEMISTRY; DERIVATIVES; ACETYLENES
- Citation
SYNLETT, no.10, pp.1511 - 1514
- ISSN
- 0936-5214
- Appears in Collection
- CH-Journal Papers(저널논문)
- Files in This Item
- There are no files associated with this item.
This item is cited by other documents in WoS
| ⊙ Detail Information in WoSⓡ | Click to see |  |
| ⊙ Cited 4 items in WoS | Click to see citing articles in |  |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.