The general formation of 1,2-trans-thioglycofuranosides derived from D-galactose, D-glucose and D-mannose was readily accomplished starting from the corresponding alkyl glycofuranosides via per-O-acetyl-hexofuranoses as key synthons. Glycosidation of ethyl or phenyl perbenzylated 1,2-transthiofurano
Short Diastereoselective Synthesis of cis- and trans-Hexahydropyrido[2,1-a]isoindole Derivatives.
β Scribed by Ala'Eddin Alsarabi; Jean-Louis Canet; Yves Troin
- Publisher
- John Wiley and Sons
- Year
- 2005
- Weight
- 26 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
Fused pyridine derivatives R 0450
Short Diastereoselective Synthesis of cis-and trans-Hexahydropyrido[2,1-a]isoindole Derivatives. -Cyclocondensation of 2-formylbenzoic acid (I) with the protected Ξ²-amino ketone (II) produces the polycyclic isoindolines (III). The latter can be transformed to a series of derivatives which represent skeletons of natural products and drugs.
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## Abstract The configuration of trans, transβ1,2βdimethyl and of trans, cisβ1, 2βdimethylethyleneβsulfite, as suggested by NMR, is in agreement with electrondiffraction results in the gas phase. The best fit to the observed diffraction intensities was obtained with a nonβplanar sulfite ring, Ο~max