Journal of Computer Chemistry, Japan
Online ISSN : 1347-3824
Print ISSN : 1347-1767
ISSN-L : 1347-1767
Letters (Selected Paper)
The Computational-chemical Study on Reactivity of Intermediates in Total Synthesis of Podophyllic Aldehydes
Yoko MIHARADai MORIKAWAYasushi NOMURAYoshinori NISHII
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2017 Volume 16 Issue 4 Pages 102-105

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Abstract

The (−)-podophyllic aldehydes (Figure 1) exhibit notable antineoplastic cytotoxicity by apoptosis-inducing activities. In this study, we analyzed the selectivity mechanisms of some important reactions in the asymmetric total synthesis of (+)-podophyllic aldehydes which are enantiomers of the (−)-podophyllic aldehydes, by the molecular orbital method. As a result, it was shown that the selectivity of the Grignard reaction in compound 1 (Figure 2) is caused by steric hindrance. Furthermore, it was also indicated that the selectivity of the reduction in compound 2–1 is caused by the localization of LUMO at the reactive site, and the reduction in compounds 2–2 and 2–3 (Scheme 2 ) does not proceed due to the steric hindrance by the trimethoxyphenyl group.

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© 2017 Society of Computer Chemistry, Japan
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