1620205-95-9Relevant academic research and scientific papers
Stepwise π-extension of meso-alkylidenyl porphyrins through sequential 1,3-dipolar cycloaddition and redox reactions
Park, Dowoo,Jeong, Seung Doo,Ishida, Masatoshi,Lee, Chang-Hee
, p. 9277 - 9280 (2014)
Several regioselectively π-extended, pyrrole fused porphyrinoids have been synthesized by the 1,3-dipolar cycloaddition of meso-alkylidene-(benzi) porphyrins. Pd(ii) complexes gave oxidation resistant, bis-pyrrole fused adducts. The repeated 1,3-dipolar c
