55160-46-8Relevant academic research and scientific papers
A metal-free one-pot cascade synthesis of highly functionalized biaryl-2-carbaldehydes
Challa, Chandrasekhar,Vellekkatt, Jamsheena,Ravindran, Jaice,Lankalapalli, Ravi S.
supporting information, p. 8588 - 8592 (2014/12/11)
A metal-free one-pot cascade annulation of acyclic substrates dienaminodioate, cinnamaldehydes and allyl amine was achieved for the synthesis of polyfunctional biaryl-2-carbaldehydes. The reaction proceeds at room temperature by a trifluoroacetic acid mediated Diels-Alder pathway. Synthetic applications of the resulting biaryl-2-carbaldehyde have been demonstrated by conversion into an array of diverse molecules with biological and materials chemistry relevance. The present work offers a complementary route to the existing metal mediated cross-coupling methods for the preparation of biaryls.
