@article{b3e460462b8047009a1360ea0ce35c9a,
title = "Intramolecular N-Me and N-H aminoetherification for the synthesis ofN-unprotected 3-amino-O-heterocycles",
abstract = "A mild Rh-catalyzed method for synthesis of cyclic unprotected N-Me and N-H 2,3-aminoethers using an olefin aziridination-aziridine ring-opening domino reaction has been developed. The method is readily applicable to the stereocontrolled synthesis of a variety of 2,3-disubstituted aminoether O-heterocyclic scaffolds, including tetrahydrofurans, tetrahydropyrans and chromanes.",
author = "Paudyal, {Mahesh P.} and Mingliang Wang and Siitonen, {Juha H.} and Yimin Hu and Muhammed Yousufuddin and Shen, {Hong C.} and Falck, {John R.} and L{\'a}szl{\'o} K{\"u}rti",
note = "Funding Information: The authors are grateful for the financial support received from Rice University, the National Institutes of Health (R35 GM-136373 for L. K., HL-139793 for J. R. F.), the National Science Foundation (CAREER:SusChEM CHE-1546097 for L. K.), the Robert A. Welch Foundation (C-1764 for L. K., I-0011 for J. R. F.), Amgen (2014 Young Investigators{\textquoteright} Award for L. K.), Biotage (2015 Young Principal Investigator Award for L. K.). J. H. S. gratefully acknowledges the support from the Osk. Huttunen Foundation. Publisher Copyright: {\textcopyright} The Royal Society of Chemistry 2021.",
year = "2021",
month = jan,
day = "21",
doi = "10.1039/d0ob02122a",
language = "English (US)",
volume = "19",
pages = "557--560",
journal = "Organic and Biomolecular Chemistry",
issn = "1477-0520",
publisher = "Royal Society of Chemistry",
number = "3",
}