76936-55-5Relevant academic research and scientific papers
Nitration of methyl eugenol derived from clove oil
Sudarma,Shofiati,Darmayanti
, p. 17 - 20 (2020)
No report is available in literature for the nitration of methyl eugenol. The main goal of this work is to find an efficient method for the synthesis of 5-nitro-methyl eugenol. 5-Nitro-methyl eugenol is of considerable importance in the production of other fine chemicals such as 5-amino-methyl eugenol for further chemical synthesis and has also possible to enhance its biological properties and other applications. The methyl eugenol can be prepared from methylation of eugenol which can be isolated from clove oil. In an attempt to synthesize nitro-methyl eugenol in high yield, three different nitration methods of methyl eugenol have been applied. Method (a) gave 5.97 %, (b) 84.37 % and (c) 11.40 %. Method (b) using a nitrating consisting mixture of HNO3 and H2SO4 under mild condition has been found to give 5-nitro-methyl eugenol in good yield.
Palladium(0)-catalyzed intramolecular decarboxylative allylation of ortho nitrobenzoic esters
Hossian, Asik,Singha, Shantanu,Jana, Ranjan
, p. 3934 - 3937 (2014/08/18)
A Pd/Ag bimetallic system has been developed for the decarboxylative allylation of ortho-nitrobenzoic esters in an intramolecular fashion. In contrast to the typical sp2-sp3 cross-coupling approach which requires air and moisture sensitive preformed organometallic reagents, we provide an alternative route to the synthesis of ortho-allyl nitroarenes from the corresponding ortho-nitrobenzoic acid derivatives. The reaction proceeds through a mechanistically distinct decarboxylative metalation pathway. A cooperative reactivity of palladium and silver is crucial for the reaction outcome.
Cyclopropyl- and allyl-substituted arenes in reaction with dinitrogen tetroxide. Effect of substrate oxidation potential on reaction direction
Mochalov,Gazzaeva,Fedotov,Trofimova,Trushkov,Zefirov
, p. 1098 - 1112 (2007/10/03)
A correlation was found between oxidation potentials of acylcyclopropanes in solution (in CH2Cl2 and CH3CN) and their HOMO energies calculated by semiempirical (AM1) and nonempirical (HF/6-31G and HF/6-31G**) methods. The
