59447-77-7Relevant articles and documents
A photoinducible 1,3-dipolar cycloaddition reaction for rapid, selective modification of tetrazole-containing proteins
Song, Wenjiao,Wang, Yizhong,Qu, Jun,Madden, Michael M.,Lin, Qing
supporting information; experimental part, p. 2832 - 2835 (2009/02/06)
(Figure Presented) Reactive but biologically inert: The bioorthogonal title reaction enables highly specific chemical modifications, such as lipidation, of engineered proteins containing a diphenyltetrazole group (see scheme). The cycloaddition in biological media is extremely fast (≤1 min) and tolerant of proteinaceous groups. Strongly fluorescent pyrazoline cycloadducts are generated with simple alkenes.
