Inherent atomic mobility changes in carbocation intermediates during the sesterterpene cyclization cascade

Hajime Sato, Takaaki Mitsuhashi, Mami Yamazaki, Ikuro Abe and Masanobu Uchiyama

Beilstein J. Org. Chem. 2019, 15, 1890–1897. doi:10.3762/bjoc.15.184

Supporting Information

Supporting Information File 1: Coordinates and energies of quiannulatene biosynthesis.
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Supporting Information File 2: Coordinates and energies of sesterfisherol biosynthesis.
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Supporting Information File 3: Software for inherent mobility analysis.
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Supporting Information File 4: How to use in house software to calculate inherent atomic mobility.
Format: PDF Size: 589.6 KB Download

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Reactive intermediates – carbocations

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