Diastereoselective Control Through Hydrogen Bonding in the Aziridination of the Chiral Allylic Alcohols by Acetoxyaminoquinazolinone
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https://figshare.com/articles/dataset/Diastereoselective_Control_Through_Hydrogen_Bonding_in_the_Aziridination_of_the_Chiral_Allylic_Alcohols_by_Acetoxyaminoquinazolinone/2805493
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资源简介：
A high diastereoselectivity (up to >99:1) is found for the aziridinations of chiral allylic alcohols with acetoxyaminoquinazolinone (Q-NHOAc). The selectivity is explained in terms of hydrogen bonding between the hydroxy functionality of the allylic alcohol and the remote carbonyl group of the quinazolinone.
创建时间：
2016-02-25
