Methoxycyclitol 4 was acetalized in a non-classical one-pot idene moiety was realised in two steps via the corresponding ethylidene acetals 8 and 9; the ethylidene function was procedure with chloral/dicyclohexylcarbodiimide forming the 4-epi derivative 6. The stepwise deprotection of removed with a
Stéréochimie de (2S, 4S, 5R;2S, 4S, 5S)- et (2R, 4S, 5R;2R, 4S, 5S)-2-alkyl-1,3,4-triméthyl-5-phénylimidazolidines déterminée par RMN-−1H et -−13C
✍ Scribed by D. Tytgat; M. Gelbcke
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 2010
- Weight
- 339 KB
- Volume
- 99
- Category
- Article
- ISSN
- 0037-9646
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✦ Synopsis
The condensation of (1 R,2S) or (lS,2S)-N,N'-dimethyI-l-phenylpropane-l 2-diamines with aldehydes gives respectively two diastereorneric 2-alkyl-l,3,4-trimethyI-S-phen limidazolidines. At thermodynamical equilibrium the major isomer in the erythro series is this one where t f ! e substituents at position 2 and 4 are "cis". In the threo series, the major isomer has the substituents at position 2 and 4 "trans".
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