123533-17-5Relevant academic research and scientific papers
Protecting-group-free route to hydroxylated pyrrolidine and piperidine derivatives through Cu(I)-catalyzed intramolecular hydroamination of alkenes
Ohmiya, Hirohisa,Yoshida, Mika,Sawamura, Masaya
scheme or table, p. 2136 - 2140 (2010/11/02)
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
Controlled Synthesis of Enantio-, Regio-, and Diastereomers of Amino-4-pentenediols from 1,4-Pentadien-ol via Epoxy-4-pentenols I. erythro-1-Amino-4-pentene-2,3-diols
Jaeger, Volker,Huemmer, Walter,Stahl, Ulrich,Gracza, Tibor
, p. 769 - 776 (2007/10/02)
erythro-1-Amino-4-pentene-2,3-diols 7, 8 of both the L- and D-series are readily accessible in high purity from 1,4-pentadien-3-ol via the 1,2-epoxy-4-pentenols 2, 4 by treatment with ammonia, primary aliphatic or aromatic amines, secondary aliphatic or a
