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An easy route to optically active 1-substituted-1-pyridyl-methylamines by diastereoselective reduction of enantiopure N-tert-butanesulfinyl ketimines

TETRAHEDRON-ASYMMETRY (2006)

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Journal

TETRAHEDRON-ASYMMETRY
Volume 17, Issue 22, Pages 3163-3169

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetasy.2006.11.026

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Categories

Chemistry, Inorganic & Nuclear Chemistry, Organic Chemistry, Physical

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The reduction of enantiopure N-tert-butanesulfinyl ketimines derived from pyridyl ketones afforded the related N-tert-but-anesulfinyl amines with high yields and diastereoselectivities. (c) 2006 Elsevier Ltd. All rights reserved.

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