Issue 16, 1987

Synergistic effect of multichiral centres. Chelation control vs. acetal template in 1,3-asymmetric induction

Abstract

The allylation of the β-siloxyacetal (5), (SR,R isomer) in the presence of TiCl4 gave the chelation adduct (6) with very high selectivity, while the (RR,R) isomer (8) also produced the chelation adduct (9), indicating that the 1,3-asymmetric induction is dictated by chelation rather than the acetal template.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1987, 1218-1219

Synergistic effect of multichiral centres. Chelation control vs. acetal template in 1,3-asymmetric induction

Y. Yamamoto and J. Yamada, J. Chem. Soc., Chem. Commun., 1987, 1218 DOI: 10.1039/C39870001218

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