Abstract
An efficient approach to hydroxylated pyrrolidine and piperidine derivatives through the intramolecular hydroamination catalyzed by a Cu(I)-Xantphos system is described. The transformation allows for the short synthesis of N-alkylated aza-sugars without a protection-deprotection event of the hydroxy groups. © Georg Thieme Verlag Stuttgart New York.
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APA
Ohmiya, H., Yoshida, M., & Sawamura, M. (2010). Protecting-group-free route to hydroxylated pyrrolidine and piperidine derivatives through Cu(I)-catalyzed intramolecular hydroamination of alkenes. Synlett, (14), 2136–2140. https://doi.org/10.1055/s-0030-1258527
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