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Photochemical ring expansion reactions: synthesis of tetrahydrofuran derivatives and mechanism studies.

ABSTRACT: The reaction mechanism of oxygen and sulfur ylide mediated rearrangements is even today a matter of debate. In this report, we describe ring expansion reactions of oxetane and thietane heterocycles that allow probing the underlying reaction mechanism under metal-free, photochemical conditions. This ring expansion proves highly efficient and allows the synthesis of tetrahydrofuran and thiolane heterocycles under mild and operationally simple reaction conditions. These studies reveal marked differences in the stereoselectivity of the ring expansion of oxygen or sulfur ylides, which were further investigated computationally. DFT calculations show that carbenes react under ylide formation and that the corresponding ring expansion reactions proceed via a diradical pathway. The different bond lengths in free oxygen or sulfur ylide intermediates cause the distinctive stereochemical outcome.

SUBMITTER: Jana S

PROVIDER: S-EPMC6968735 | biostudies-literature | 2019 Nov

REPOSITORIES: biostudies-literature

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Photochemical ring expansion reactions: synthesis of tetrahydrofuran derivatives and mechanism studies.

Jana Sripati S Yang Zhen Z Pei Chao C Xu Xinfang X Koenigs Rene M RM

Chemical science 20190906 43

The reaction mechanism of oxygen and sulfur ylide mediated rearrangements is even today a matter of debate. In this report, we describe ring expansion reactions of oxetane and thietane heterocycles that allow probing the underlying reaction mechanism under metal-free, photochemical conditions. This ring expansion proves highly efficient and allows the synthesis of tetrahydrofuran and thiolane heterocycles under mild and operationally simple reaction conditions. These studies reveal marked differ ...[more]

PMID: 32015819

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