Journal article

Carbon‐to‐Carbon Anion Relay Chemistry: Facile Generation of Substituted Allyllithium Species


Authors listZheng, P; Cai, Z; A, Garimallaprabhakaran; Rooshenas, P; Schreiner, PR; Harmata, M

Publication year2011

Pages5255-5260

JournalEuropean Journal of Organic Chemistry

Volume number2011

Issue number27

DOI Linkhttps://doi.org/10.1002/ejoc.201100783

PublisherWiley


Abstract

Treatment of [2‐(2‐bromophenyl)allyl]trimethylsilane with tBuLi in
THF at –78 °C resulted in the rapid migration of the trimethylsilyl
group to afford an allylic organolithium that can be easily trapped by a
wide range of electrophiles. This is a rare example of a synthetically
useful and efficientcarbon‐to‐carbon migration of a silicon group and
represents a new approach to allylic organolithium species using anion
relay chemistry.




Citation Styles

Harvard Citation styleZheng, P., Cai, Z., A, G., Rooshenas, P., Schreiner, P. and Harmata, M. (2011) Carbon‐to‐Carbon Anion Relay Chemistry: Facile Generation of Substituted Allyllithium Species, European Journal of Organic Chemistry, 2011(27), pp. 5255-5260. https://doi.org/10.1002/ejoc.201100783

APA Citation styleZheng, P., Cai, Z., A, G., Rooshenas, P., Schreiner, P., & Harmata, M. (2011). Carbon‐to‐Carbon Anion Relay Chemistry: Facile Generation of Substituted Allyllithium Species. European Journal of Organic Chemistry. 2011(27), 5255-5260. https://doi.org/10.1002/ejoc.201100783


Last updated on 2025-21-05 at 13:31