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Isotope Effects, Dynamic Matching, and Solvent Dynamics in a Wittig Reaction. Betaines as Bypassed Intermediates

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TLDR
The mechanism of the Wittig reaction of anisaldehyde with a stabilized ylide was studied by a combination of 13C kinetic isotope effects, conventional calculations, and molecular dynamics calculations in a cluster of 53 THF molecules.
Abstract
The mechanism of the Wittig reaction of anisaldehyde with a stabilized ylide was studied by a combination of 13C kinetic isotope effects, conventional calculations, and molecular dynamics calculations in a cluster of 53 THF molecules. The isotope effects support a cycloaddition mechanism involving two sequential transition states associated with separate C–C and P–O bond formations. However, the betaine structure in between the two transition states is bypassed as an equilibrated intermediate in most trajectories. The role of the dynamics of solvent equilibration in the nature of mechanistic intermediates is discussed.

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Direct Chemical Dynamics Simulations.

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Post-transition state bifurcations gain momentum – current state of the field

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Dynamics and the Regiochemistry of Nitration of Toluene.

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Cryptic post-transition state bifurcations that reduce the efficiency of lactone-forming Rh-carbenoid C–H insertions

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Unified Mechanistic Understandings of Pictet-Spengler Reactions

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References
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Book

The tunnel effect in chemistry

TL;DR: In this article, the authors present a review of the present position of the tunnel correction for a parabolic barrier and the application of tunnel corrections in chemical kinetics, as well as the theory of kinetic isotope effects.
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The Relative Reaction Velocities of Isotopic Molecules

TL;DR: In this article, the rate constants for competitive reactions of isotopic molecules are considered from the theory of ''absolute rates'' and the collision theory, and the conditions for the rate constant of the heavy molecule to exceed that of the light one are formulated.
Journal ArticleDOI

A SN2 Reaction That Avoids Its Deep Potential Energy Minimum

TL;DR: The finding that the majority of trajectories avoided this potential energy minimum and instead dissociated directly to products and may be applicable to other reactive systems where there is a hierarchy of time scales for intramolecular motions and thus inefficient IVR.
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The modern interpretation of the Wittig reaction mechanism

TL;DR: It is made the case that a clear distinction should henceforth be made between the unknown "Li-present" and the now well-established "Li salt-free" Wittig mechanisms.
Journal ArticleDOI

Dynamic effects on the periselectivity, rate, isotope effects, and mechanism of cycloadditions of ketenes with cyclopentadiene.

TL;DR: An understanding of the products, rates, selectivities, isotope effects, and mechanism in these reactions requires the explicit consideration of dynamic trajectories.
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