Applications synthétiques de la cyclisation d'alcools tertiaires γ‐éthyléniques en α‐bromotétrahydrofurannes sous l'action du N‐bromosuccinimide. I. Synthèse facile de la triméthyl‐2,2,5‐cycloheptène‐4‐one ou karahanaénone à partir du linalol
- 1 January 1971
- journal article
- research article
- Published by Wiley in Helvetica Chimica Acta
- Vol. 54 (2) , 456-463
- https://doi.org/10.1002/hlca.19710540204
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Claisen rearrangement of 3,4-dihydro-2H-pyranylethylenes. Synthesis of cyclohexenesJournal of the American Chemical Society, 1970
- Synthesewege zum 17α‐Hydroxy‐16‐methylen‐19‐nor‐progesteron und seinen DerivatenEuropean Journal of Inorganic Chemistry, 1969
- Bromohydrin formation in dimethyl sulfoxideJournal of the American Chemical Society, 1968
- Volatile Constituents of Hops (Part II)Nippon kagaku zassi, 1968
- Thermal Rearrangement of 2,5-Dimethyl-2-vinyl-2,3-dihydrofuran to 4-Methyl-4-cycloheptenoneJournal of the American Chemical Society, 1966
- Die Chemie der Linalool‐oxideEuropean Journal of Organic Chemistry, 1964
- Zur Kenntnis ätherischer Öle. 2. Mitteilung. Die Struktur der sogenannten «Linalooloxide»Helvetica Chimica Acta, 1963
- N-Bromosuccinimide. I. Allylic Bromination, a General Survey of Reaction Variables1-3Journal of the American Chemical Society, 1959
- The Stereochemistry of Elimination Reactions Involving Halohydrin Derivatives and Metals1Journal of the American Chemical Society, 1958