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Ring Expansion of Cyclic β-Amino Alcohols Induced by Diethylaminosulfur Trifluoride: Synthesis of Cyclic Amines with a Tertiary Fluorine at C3

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NIAID Data Ecosystem2026-03-07 收录
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https://figshare.com/articles/dataset/Ring_Expansion_of_Cyclic_Amino_Alcohols_Induced_by_Diethylaminosulfur_Trifluoride_Synthesis_of_Cyclic_Amines_with_a_Tertiary_Fluorine_at_C3/2503336
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As the replacement of a hydrogen atom by a fluorine atom in a compound can have an important impact on its biological properties, the development of methods allowing the introduction of a fluorine atom is of great importance. The scope and limitations of the ring expansion of cyclic 2-hydroxymethyl amines induced by diethylaminosulfur trifluoride (DAST) to produce cyclic β-fluoro amines was studied as well as the enantioselectivity of the process.
创建时间:
2016-02-20
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