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• Asymmetric Synthesis, Chemical Synthesis, Chiral Building Blocks, Organic Building Blocks, Polyols
• {SA} Analytical Reagents, Analytical/Chromatography, Asymmetric Synthesis, Chemical Synthesis, Chiral, Chiral Building Blocks, Derivatization Reagents, Derivatization Reagents HPLC, Organic Building Blocks, Polyols
• {SNA} Asymmetric Synthesis, Chemical Synthesis, Chiral Building Blocks, Organic Building Blocks, Polyols
• {uni_hamburg} no charge; alcohol; chiral; 1fragment

相关文献及参考

• Has been used for the resolution and determination of enantiomeric excess of chiral ketones by formation of the cyclic acetal and 13C-NMR: Tetrahedron Lett., 2183 (1977); J. Am. Chem. Soc., 109, 1363 (1987).
• Similarly, acetals react with Li organocuprates in the presence BF3 etherate to give only one of the two possible enantiomeric ethers: Tetrahedron, 45, 507 (1989):
• Forms cyclic acetals with aldehydes, which have been used in an enantioselective Lewis acid catalyzed aldol condensation: J. Am. Chem. Soc., 104, 7371,7372 (1982); Tetrahedron, 40, 4685 (1984):
• With boronic acids forms
• With boronic acids forms cyclic boronates, useful in asymmetric syntheses; reviews: Acc. Chem. Res., 21, 294 (1988); Te
• With boronic acids forms cyclic boronates, useful in asymmetric syntheses; reviews: Acc. Chem. Res., 21, 294 (1988); Tetrahedron, 45, 1859 (1989). See Appendix 5.

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