@article {43616,
	title = {Proline catalyzed enantioselective synthesis of (2S,3S)-3-hydroxypipecolic acid and formal synthesis of (+)-swainsonine},
	journal = {Tetrahedron Letters},
	volume = {57},
	year = {2016},
	month = {MAY},
	pages = {2021-2024},
	abstract = {A short enantioselective synthesis of (2S,3S)-3-hydroxypipecolic acid (overall yield: 18.8\%; 96\% ee) and formal synthesis of (+)-swainsonine (overall yield: 13.6\%; 96\% ee) have been described starting from commercially available acrolein. The synthetic strategy involves a high enantioselective L-proline catalyzed sequential c-amination and diastereoselective (dr > 99:1) Barbier allylation of aldehyde in one-pot as the key reaction. (C) 2016 Elsevier Ltd. All rights reserved.},
	doi = {10.1016/j.tetlet.2016.03.042},
	author = {Aher, Ravindra D. and Sudalai, Arumugam}
}
