Corrigendum to “Convenient synthesis of enantiopure (R-) and (S-)-3-fluoro-3-aminomethylpyrrolidines” [Tetrahedron 70 (2014) 3011–3017]

[3+2] Cycloaddition of an Azomethyne Ylide and Vinyl Sulfonyl Fluorides ― an Approach to Pyrrolidine‐3‐sulfonyl Fluorides

“…TFA (trifluoroacetic acid), room temp. }, which was originally developed by Achiwa and coworkers, and has been widely used by us and others in recent years, could be used for a reaction with the parent commercially available vinyl sulfonyl fluoride 1a (Scheme , R 1 = R 2 = H). We found that under these typical conditions, the target adduct 3a was obtained in 75 % yield (Table ).…”