Organoytterbium ate complexes extend the value of cyclobutenediones as isoprene equivalents

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Abstract

Changing course: While organolithium and Grignard reagents favor addition to C1 of A (R=Me), the corresponding organoytterbium reagents add to C2 (R=tBu). Computational studies provide insights into the nature of organoytterbium species and their reactivity, and a total synthesis of (-)-mansonone B illustrates the utility of the method in terpenoid synthesis. Tf=trifluoromethanesulfonyl. © 2013 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.

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Packard, E., Pascoe, D. D., Maddaluno, J., Gonçalves, T. P., & Harrowven, D. C. (2013). Organoytterbium ate complexes extend the value of cyclobutenediones as isoprene equivalents. Angewandte Chemie - International Edition, 52(49), 13076–13079. https://doi.org/10.1002/anie.201307193

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