IODOETHERIFICATION OF CONFORMATIONALLY RESTRICTED DIENYL ALCOHOLS: UNEXPECTED FORMATION OF OXOCENES BY 9-ENDO-MODE OXACYCLIZATIONS

Kristen L. Stoltz; Andrea-Nekane R. Alba; Frank E. McDonald

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IODOETHERIFICATION OF CONFORMATIONALLY RESTRICTED DIENYL ALCOHOLS: UNEXPECTED FORMATION OF OXOCENES BY 9-ENDO-MODE OXACYCLIZATIONS

机译：构型受限的二苯基醇的碘代醚化反应：9-内位模式羰基化法意外形成了茂金属

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Iodine-promoted oxacydizations of a family of conformationally restricted dienyl alcohols consistently afford oxocenes, arising from 8-endo-mode cyclizations.

机译：构象受限的二烯基醇家族的碘促进的氧酰化作用始终产生由8-内-模式环化产生的茂茂化合物。

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《Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry》 |2014年第2期|共8页
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Kristen L. Stoltz; Andrea-Nekane R. Alba; Frank E. McDonald;
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1. IODOETHERIFICATION OF CONFORMATIONALLY RESTRICTED DIENYL ALCOHOLS: UNEXPECTED FORMATION OF OXOCENES BY 9-ENDO-MODE OXACYCLIZATIONS [J] . Kristen L. Stoltz, Andrea-Nekane R. Alba, Frank E. McDonald Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry . 2014,第2期

机译：构型受限的二苯基醇的碘代醚化反应：9-内位模式羰基化法意外形成了茂金属
2. Transformation of C-4-Methyl Derivatives of Levoglucosenone to 2,5-Dihydrofurans. An Unexpected Intramolecular Oxacyclization [J] . Russian Journal of Organic Chemistry . 2019,第11期

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IODOETHERIFICATION OF CONFORMATIONALLY RESTRICTED DIENYL ALCOHOLS: UNEXPECTED FORMATION OF OXOCENES BY 9-ENDO-MODE OXACYCLIZATIONS

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