96254-09-0Relevant articles and documents
Coupling of C(sp3)-H bonds with C(sp2)-O electrophiles: mild, general and selective
Gui, Yong-Yuan,Liao, Li-Li,Sun, Liang,Zhang, Zhen,Ye, Jian-Heng,Shen, Guo,Lu, Zhi-Peng,Zhou, Wen-Jun,Yu, Da-Gang
supporting information, p. 1192 - 1195 (2017/02/05)
Herein is reported the mild and general coupling of amine/ether C(sp3)-H bonds with various kinds of C(sp2)-O electrophiles with high selectivity and efficiency. Valuable allylic/benzylic amines are generated in moderate to excellent yields. The utility of this transformation is demonstrated by a broad substrate scope (>50 examples), good functional group tolerance and facile product modification.
A new one-pot solvent-free synthesis of pyridinyl tosylates via diazotization of aminopyridines
Tretyakov, Alexey N.,Krasnokutskaya, Elena A.,Gorlushko, Dmitry A.,Ogorodnikov, Vladimir D.,Filimonov, Victor D.
supporting information; experimental part, p. 85 - 87 (2011/02/25)
A new, convenient, one-pot method for the synthesis of pyridinyl tosylates is developed. The procedure involves sequential diazotization/tosylation of aminopyridines with sodium nitrite and p-toluenesulfonic acid under solvent-free conditions in a water p