1972
DOI: 10.1002/chin.197228308
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ChemInform Abstract: SYNTH. UND UNTERSUCHUNGEN 2,4,5‐TRISUBSTITUIERTER 1,3‐DIOXOLANE

Abstract: Die p‐Toluolsulfonsäure‐katalysierte Umsetzung von meso‐ bzw. threo‐Äthylenglykol (Ia) und von (RR)(‐)‐ bzw. meso‐Dimethyltartrat (Ib) mit den Aldehyden (II) zu den Dioxolanen (III) (oft als Stereoisomerengemische) wird beschrieben.

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“…Four configurational isomers can be drawn assuming a planar conformation of the 1,3-dioxolane ring (Figure 11). 42,43,44 The 4R,5Rand the 4S,5S-isomers have optical activity. The others represent meso forms with (R,S) and (S,R) configurations at the carbon atoms 4 and 5, and pseudo-chirality at position 2.…”
Section: Nuclear Overhauser Effectmentioning
confidence: 99%
“…Four configurational isomers can be drawn assuming a planar conformation of the 1,3-dioxolane ring (Figure 11). 42,43,44 The 4R,5Rand the 4S,5S-isomers have optical activity. The others represent meso forms with (R,S) and (S,R) configurations at the carbon atoms 4 and 5, and pseudo-chirality at position 2.…”
Section: Nuclear Overhauser Effectmentioning
confidence: 99%