(S,S)-3,5-Dimethylmorpholine, a NovelC 2-Symmetric Auxiliary. First Application in [4+2]-Cycloadditions Leading to 4-Oxohexahydropyridazine Derivatives
- 1 January 1994
- journal article
- research article
- Published by Georg Thieme Verlag KG in Synthesis
- Vol. 1994 (01) , 66-72
- https://doi.org/10.1055/s-1994-25407
Abstract
Diastereoselective Diels-Alder reactions of (S,S)-2-(3,5-dimethylmorpholino) butadienes 10 with aza-dienophiles are described, leading to cycloadducts 12 in good yields and high stereoselectivities (de = 87-96%). After double bond migration to 13, acidic and basic hydrolysis affords 4-oxohexahydropyridazine derivatives 14 and 16 of high enantiomeric purity (ee = 90-91%). The configuration of the new stereogenic centre is determined by NOE-measurements and an X-ray structure analysis of the cycloadduct (R,S,S)- 13f.Keywords
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