Protecting-group-free route to hydroxylated pyrrolidine and piperidine derivatives through Cu(I)-catalyzed intramolecular hydroamination of alkenes

20Citations
Citations of this article
15Readers
Mendeley users who have this article in their library.

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.

Cite

CITATION STYLE

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

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free