Inherent dynamical preferences in carbocation rearrangements leading to terpene natural products

Ryan P. Pemberton; Young J. Hong; Dean J. Tantillo

doi:10.1351/pac-con-12-11-22

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Inherent dynamical preferences in carbocation rearrangements leading to terpene natural products

Ryan P. Pemberton , Young J. Hong and Dean J. Tantillo

Published/Copyright: July 10, 2013

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From the journal Pure and Applied Chemistry Volume 85 Issue 10

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Pemberton, Ryan P., Hong, Young J. and Tantillo, Dean J.. "Inherent dynamical preferences in carbocation rearrangements leading to terpene natural products" Pure and Applied Chemistry, vol. 85, no. 10, 2013, pp. 1949-1957. https://doi.org/10.1351/pac-con-12-11-22

Pemberton, R., Hong, Y. & Tantillo, D. (2013). Inherent dynamical preferences in carbocation rearrangements leading to terpene natural products. Pure and Applied Chemistry, 85(10), 1949-1957. https://doi.org/10.1351/pac-con-12-11-22

Pemberton, R., Hong, Y. and Tantillo, D. (2013) Inherent dynamical preferences in carbocation rearrangements leading to terpene natural products. Pure and Applied Chemistry, Vol. 85 (Issue 10), pp. 1949-1957. https://doi.org/10.1351/pac-con-12-11-22

Pemberton, Ryan P., Hong, Young J. and Tantillo, Dean J.. "Inherent dynamical preferences in carbocation rearrangements leading to terpene natural products" Pure and Applied Chemistry 85, no. 10 (2013): 1949-1957. https://doi.org/10.1351/pac-con-12-11-22

Pemberton R, Hong Y, Tantillo D. Inherent dynamical preferences in carbocation rearrangements leading to terpene natural products. Pure and Applied Chemistry. 2013;85(10): 1949-1957. https://doi.org/10.1351/pac-con-12-11-22

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Published Online: 2013-7-10

Published in Print: 2013-10-1

Articles in the same Issue

Preface
The interplay of thermodynamics and kinetics in dictating organocatalytic reactivity and selectivity
Inherent dynamical preferences in carbocation rearrangements leading to terpene natural products
Rearrangements in the mechanisms of the indole alkaloid prenyltransferases
The structure of halonium ions in superacidic solutions
Recent progress in research on stimuli-responsive circularly polarized luminescence based on π-conjugated molecules
Towards solvent-controlled reactivity in ionic liquids
A new reaction mechanism of Claisen rearrangement induced by few-optical-cycle pulses: Demonstration of nonthermal chemistry by femtosecond vibrational spectroscopy
Determination of the photoluminescence quantum yield of dilute dye solutions (IUPAC Technical Report)

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https://doi.org/10.1351/pac-con-12-11-22

Articles in the same Issue

Preface
The interplay of thermodynamics and kinetics in dictating organocatalytic reactivity and selectivity
Inherent dynamical preferences in carbocation rearrangements leading to terpene natural products
Rearrangements in the mechanisms of the indole alkaloid prenyltransferases
The structure of halonium ions in superacidic solutions
Recent progress in research on stimuli-responsive circularly polarized luminescence based on π-conjugated molecules
Towards solvent-controlled reactivity in ionic liquids
A new reaction mechanism of Claisen rearrangement induced by few-optical-cycle pulses: Demonstration of nonthermal chemistry by femtosecond vibrational spectroscopy
Determination of the photoluminescence quantum yield of dilute dye solutions (IUPAC Technical Report)