Csp3–Csp3 and Csp3–H Bond Activation of 1,1-Disubstituted Cyclopentane
收藏Figshare2016-02-20 更新2026-04-29 收录
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https://figshare.com/articles/dataset/C_sub_sp_sup_3_sup_sub_C_sub_sp_sup_3_sup_sub_and_C_sub_sp_sup_3_sup_sub_H_Bond_Activation_of_1_1_Disubstituted_Cyclopentane/2464072
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资源简介：
The unprecedented Csp3–Csp3 bond cleavage of unactivated cyclopentane has been achieved. RhI-catalyzed cycloaddition of allenylcyclopentane-alkynes produced in situ the 9-cyclopentyl-8-rhodabicyclo[4.3.0]nona-1,6-diene intermediates, which subsequently underwent [7+2] cycloaddition via β-C elimination, affording bicyclo[7.4.0]tridecatriene derivatives in good yields. Changing the RhI catalyst effected the Cγ–H bond activation of the common 9-cyclopentyl-8-rhodabicyclo[4.3.0]nona-1,6-diene intermediate to produce the novel spiro[2.4]heptane skeleton in a site-selective manner.
创建时间：
2016-02-20
