Abstract
The synthesis of monomers for the production of novel green polymers was evaluated in continuous flow conditions using terpenes as dienes and maleic anhydride as dienophile for the [4+2] Diels-Alder cycloaddition reaction. The hydrogenation reaction was also evaluated to prevent the retro-Diels-Alder and to expand the reactional scope by producing adducts with distinct characteristics of structures and reactivity. Fourteen different monomers were obtained in good yields in flow regime.

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Copyright (c) 2019 Lucas Pera Fernandes, Julio Cezar Pastre