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Development of a Chiral Bis(guanidino)iminophosphorane as an Uncharged Organosuperbase for the Enantioselective Amination of Ketones

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NIAID Data Ecosystem2026-03-07 收录
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https://figshare.com/articles/dataset/Development_of_a_Chiral_Bis_guanidino_iminophosphorane_as_an_Uncharged_Organosuperbase_for_the_Enantioselective_Amination_of_Ketones/2366023
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Chiral bis­(guanidino)­imino­phosphoranes were designed and synthesized as chiral uncharged organo­superbase catalysts that facilitate activation of less-acidic pro-nucleophiles. The newly developed bis­(guanidino)­imino­phosphoranes, which possess the highest basicity among chiral organocatalysts reported to date, were proven to be a superb class of chiral organo­superbases by reaction of azodicarboxylates with 2-alkyltetralones and their analogues as the less acidic pro-nucleophiles.
创建时间:
2013-10-16
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