## Studies of π-Diastereofacial Selectivity: The Influence of α-Oxathiolane Ketals on Cyclic Ketones. -The addition reaction of organometals (II) or hydride reagents to the carbonyl of the α-keto-oxathiolane ketals (I) and (V) occurs preferentially via attack anti to sulfur and syn to oxygen. How
Studies of π-diastereofacial selectivity: The influence of α-oxathiolane ketals on cyclic ketones
✍ Scribed by Martin Dimitroff; Alex G Fallis
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 238 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0040-4039
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📜 SIMILAR VOLUMES
We describe the preliminary results of manganese(III) acetate based selective oxidation of various a%-methyl 2-cyclohexenone and 2-cyclopentenone derivatives to afford the corresponding a%-acetoxy-a%-methyl substituted oxidation products in good yields.
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