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Synlett 2005(13): 2101-2103
DOI: 10.1055/s-2005-871956
DOI: 10.1055/s-2005-871956
LETTER
© Georg Thieme Verlag Stuttgart · New York
Rapid Access to trans-2,6-Disubstituted Piperidines: Expedient Total Syntheses of (-)-Solenopsin A and (+)-epi-Dihydropinidine
Further Information
Received
4 May 2005
Publication Date:
12 July 2005 (online)
Publication History
Publication Date:
12 July 2005 (online)
Abstract
Expedient syntheses of (-)-solenopsin A and (+)-epi-dihydropinidine are reported, the key step in both being the one-pot multicomponent aza-silyl-Prins condensation reaction to yield a trans dihydropyridine.
Key words
total synthesis - (-)-solenopsin A - (+)-epi-dihydropinidine - multicomponent condensation - aza-silyl-Prins reaction - trans dihydropyridine
- 1
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References
All compounds gave satisfactory analytical and spectroscopic data. Data for 7 and 8 in agreement with previously reported values.2,3
7The absence of racemisation of compounds 4-8 was judged by NMR experiments using Eu(hfc)3 doping at each stage and comparison with the racemic series, where separation occurred.