Silyl Tosylate Precursors to Cyclohexyne, 1,2-Cyclohexadiene, and 1,2-Cycloheptadiene

被引:17
作者
McVeigh, Matthew S. [1 ]
Kelleghan, Andrew, V [1 ]
Yamano, Michael M. [1 ]
Knapp, Rachel R. [1 ]
Garg, Neil K. [1 ]
机构
[1] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
基金
美国国家科学基金会;
关键词
DIELS-ALDER REACTION; GENERATION; ARYNES; CYCLOADDITIONS; REARRANGEMENT; INTERMEDIATE; CHEMISTRY; TRIFLATE; BENZYNE;
D O I
10.1021/acs.orglett.0c01510
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Transient strained cyclic intermediates have become valuable intermediates in modern synthetic chemistry. Although silyl triflate precursors to strained intermediates are most often employed, the instability of some silyl triflates warrants the development of alternative precursors. We report the syntheses of silyl tosylate precursors to cyclohexyne, 1,2-cyclohexadiene, and 1,2-cydoheptadiene. The resultant strained intermediates undergo trapping in situ to give cycloaddition products. Additionally, the results of competition experiments between silyl triflates and silyl tosylates are reported.
引用
收藏
页码:4500 / 4504
页数:5
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