Synthesis of enantiomerically pure (5S)-4-aza-2-oxa-6,6-dimethyl-7,10-methylene-5-spiro[4.5]decan-3-one, a novel chiral oxazolidin-2-one from (-)-camphene for use as a recyclable chiral auxiliary in asymmetric transformations
- Author
- BANKS, M. R1 ; CADOGAN, J. I. G; GOSNEY, I1 ; GRANT, K. J1 ; HODGSON, P. K. G; THORBURN, P1
[1] Univ. Edinburgh, dep. chemistry, Edinburgh EH9 3JJ, United Kingdom - Source
Heterocycles (Sendai). 1994, Vol 37, Num 1, pp 199-206 ; ref : 13 ref
- CODEN
- HTCYAM
- ISSN
- 0385-5414
- Scientific domain
- Organic chemistry
- Publisher
- Elsevier, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Auxiliaire chiral Carbamate organique Carbonyle Chlorure Hydrogène Peroxyde Monoterpène Réaction asymétrique Spirane Norbornane(2,2-diméthyl-3-méthylène) Spiro[norbornane-2:4p-oxazolidin-2p-one](3,3-diméthyl)
- Keyword (en)
- Chiral auxiliary Organic carbamate Carbonyl Chlorides Hydrogen Peroxides Monoterpene Asymmetric reaction Spiran
- Keyword (es)
- Auxiliar quiral Carbamato orgánico Carbonilo Cloruro Hidrógeno Peróxido Monoterpeno Reacción asimétrica Espirano
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06D Heterocyclic compounds with n hetero atom and also o and/or s, se, te hetero atoms
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 3905110
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.3987/COM-93-S28 
https://dx.doi.org/10.3987/COM-93-S28
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