257630-75-4Relevant academic research and scientific papers
N-Benzyl-N-(2-iodo-4-methylphenyl)-cinnamamide and N-benzyl-N-(p-tolyl)-cinnamamide
Shanmuga Sundara Raj,Renganayaki,Subramanian,Fun, Hoong-Kun
, p. 2182 - 2184 (1999)
The cinnamamide moiety in the crystals of the title compounds, C23H20INO, (I), and C23H21NO, (II), is almost planar and the benzyl ring is twisted through 60.4(4) and 63.6(1)° with respect to this moiety in (I)
Cathodic reduction of N-(2-iodophenyl)-N-alkylcinnamides: A novel sequential electrochemical radical cyclisation and hydroxylation
Munusamy, Raja,Dhathathreyan, Kaveripatnam Samban,Balasubramanian, Kalpattu Kuppusamy,Venkatachalam, Chitoor Sivaramakrishnan
, p. 1154 - 1166 (2007/10/03)
In recent years, intramolecular aryl radical cyclisation has emerged as a useful route for the synthesis of benzannulated heterocycles and carbocycles. The aryl radicals are generated in situ from aryl halides (iodides or bromides) with tributylstannyl hydride-AIBN, SmI2, Co(I) or under photochemical conditions. The present work envisages the generation of aryl radicals by cathodic reduction of the carbon-iodine bond of N-(2-iodophenyl)-N-alkylcinnamides and their intramolecular cyclisation. The cathodic reduction of N-(2-iodophenyl)-N-alkyl-cinnamides under deaerated conditions in DMF gave 1-alkyl-3-benzylindolin-2-ones regioselectively and in the presence of oxygen yielded surprisingly 1-alkyl-3-hydroxy-3-benzylindolin-2-ones. Both these products were formed by a 5-exo-trig process in good yields. A mechanism for the formation of the products has been proposed through the use of cyclic voltammetry, coulometry and controlled-potential electrolysis as well as deuterium labelling.
