Lopes, Susana M. M.Lemos, A.Melo, Teresa M. V. D. Pinho e2012-04-182012-04-182010Lopes, Susana M.M.; Lemos, A.; Melo, Teresa M.V.D. Pinho e. A hetero-Diels–Alder approach to functionalized 1H-tetrazoles: synthesis of tetrazolyl-1,2-oxazines, -oximes and 5-(1-aminoalkyl)-1H-tetrazoles. Tetrahedron Letters, 51, 51, 6756-6759, 2010.00404039AUT: ALE01411;http://hdl.handle.net/10400.1/1041This work describes the first and unprecedented examples of inverse electron demand Diels–Alder reactions of 5-(1-nitrosovinyl)-1-phenyl-1H-tetrazole, generated in situ from the corresponding bromooxime, with electron rich alkenes and heterocycles, providing in good overall yields tetrazolyl- 1,2-oxazines and -oximes. Upon subsequent reduction these allowed the access to 5-(1-aminoalkyl)- 1H-tetrazoles, paving the way for a new entry into this important class of compounds, bioisosteres of a-amino acids.eng5-(1-Aminoalkyl)-1H-tetrazolesNitrosovinyltetrazoleCycloadditionOximeOxazineA hetero-Diels–Alder approach to functionalized 1H-tetrazoles: synthesis of tetrazolyl-1,2-oxazines, -oximes and 5-(1-aminoalkyl)-1H-tetrazolesjournal article2012-04-13