Spectral data for the synthesis of (E)-alkenylboronic acid pinacol esters via hydroboration of alkynes
Bruna Gioia,
Alexandre Arnaud,
Sylvie Radix,
Nadia Walchshofer,
Anne Doléans-Jordheim,
Luc Rocheblave
Affiliations
Bruna Gioia
Univ Lyon, Université Claude Bernard Lyon 1, ISPB-Faculté de Pharmacie, EA 4446, B2MC, F-69373, Lyon Cedex 08, France
Alexandre Arnaud
Univ Lyon, Université Claude Bernard Lyon 1, ISPB-Faculté de Pharmacie, EA 4446, B2MC, F-69373, Lyon Cedex 08, France
Sylvie Radix
Univ Lyon, Université Claude Bernard Lyon 1, ISPB-Faculté de Pharmacie, EA 4446, B2MC, F-69373, Lyon Cedex 08, France
Nadia Walchshofer
Univ Lyon, Université Claude Bernard Lyon 1, ISPB-Faculté de Pharmacie, EA 4446, B2MC, F-69373, Lyon Cedex 08, France
Anne Doléans-Jordheim
Univ Lyon, Université Claude Bernard Lyon 1, VetAgro Sup, UMR CNRS 5557, Ecologie Microbienne, F-69622, Villeurbanne, France; Laboratoire de Bactériologie, Centre de Biologie et Pathologie Est, Hospices Civils de Lyon (HCL), F-69000, Bron, France
Luc Rocheblave
Univ Lyon, Université Claude Bernard Lyon 1, ISPB-Faculté de Pharmacie, EA 4446, B2MC, F-69373, Lyon Cedex 08, France; Corresponding author.
This data article is related to a research paper entitled “Solvent- and metal-free hydroboration of alkynes under microwave irradiation” (Gioia et al. TETL-D-19-01698) [1]. Herein we present the spectral data acquired from the synthesis of (E)-alkenyl boronic acid pinacol esters. The data include the general information and the synthetic procedure affording the target derivatives, which were fully characterized by Nuclear Magnetic Resonance (1H and 13C NMR) and, for the most part, by Electrospray Ionization High Resolution Mass (ESI-MS). Proton and carbon NMR spectra and ESI-MS spectra were provided which will be useful for further organic chemists if they are interested in the synthesis of these building blocks.