Discrimination of cryptochirality in chiral isotactic polystyrene by asymmetric autocatalysis

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Abstract

Chiral isotactic polystyrenes induce the enantioselective addition of diisopropylzinc to pyrimidine-5-carbaldehyde, affording the enantiomerically enriched pyrimidyl alkanol with the corresponding absolute configuration to that of cryptochiral polystyrenes in conjunction with asymmetric autocatalysis. © 2009 The Royal Society of Chemistry.

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APA

Kawasaki, T., Hohberger, C., Araki, Y., Hatase, K., Beckerle, K., Okuda, J., & Soai, K. (2009). Discrimination of cryptochirality in chiral isotactic polystyrene by asymmetric autocatalysis. Chemical Communications, (37), 5621–5623. https://doi.org/10.1039/b912813a

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