Structural Reevaluation of the Electrophilic Hypervalent Iodine Reagent for Trifluoromethylthiolation Supported by the Crystalline Sponge Method for X-ray Analysis

被引:206
作者
Vinogradova, Ekaterina V. [1 ]
Mueller, Peter [1 ]
Buchwald, Stephen L. [1 ]
机构
[1] MIT, Dept Chem, Cambridge, MA 02139 USA
基金
美国国家科学基金会;
关键词
crystalline sponge crystallography; host-guest systems; hypervalent compounds; thioperoxides; trifluoromethylthiolation; DIRECT ALKYNYLATION; BENZIODOXOLONES; PROTOCOL; ACIDS; GOLD; EBX;
D O I
10.1002/anie.201310897
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hypervalent iodine (3)-benziodoxoles are common electrophilic transfer reagents known for their enhanced stability compared to their non-cyclic analogues. Herein we present data showing that chlorobenziodoxole reacts with two different thiolate nucleophiles (thiocyanate and trifluoromethylthiolate), resulting in the formation of stable thioperoxy complexes rather than the expected benziodoxole derivatives. We further report a revised structure for the earlier described electrophilic trifluoromethylthiolation reagent (1), which was previously believed to contain the benziodoxole framework. Our findings, which are based on a combination of analytical techniques, including the recently introduced crystalline sponge method for X-ray analysis, unambiguously demonstrate that 1 is a thioperoxy compound both in solution and the solid state.
引用
收藏
页码:3125 / 3128
页数:4
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