Synthesis of 2-Benzylphenyl Ketones by Aryne Insertion into Unactivated C–C Bonds
摘要:
A transition-metal-free procedure to access to functionalized 2-benzylphenyl ketones is described by direct insertion of arynes into benzylic C-C bonds. This reaction was promoted by cesium fluoride at room temperature, allowing the products to form in high selectivity and achieve good functional group tolerance.
Aromatic Cyclodehydration. XXII.<sup>1</sup> The Mechanism of the Cyclization of <i>o</i>-Benzylphenones. III
作者:Charles K. Bradsher、Frank A. Vingiello
DOI:10.1021/ja01172a082
日期:1949.4
Synthesis of 2-Benzylphenyl Ketones by Aryne Insertion into Unactivated C–C Bonds
作者:Bin Rao、Jinghua Tang、Xiaoming Zeng
DOI:10.1021/acs.orglett.6b00578
日期:2016.4.1
A transition-metal-free procedure to access to functionalized 2-benzylphenyl ketones is described by direct insertion of arynes into benzylic C-C bonds. This reaction was promoted by cesium fluoride at room temperature, allowing the products to form in high selectivity and achieve good functional group tolerance.
1,4-DIARYLPHTHALAZINES AND 1,3-DIARYLISOBENZOFURANS