Journal
TETRAHEDRON-ASYMMETRY
Volume 14, Issue 5, Pages 581-586Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0957-4166(03)00024-7
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A short and efficient enantioselective synthesis of (R)-(-)-baclofen, a selective GABA(B) agonist has been described with an overall yield of 26% and 90% ee. Ru(II)-(S)-BINAP catalyzed asymmetric hydrogenations of C=C and C=O groups constitute the key steps in introducing stereogenic centers into the molecule. (C) 2003 Elsevier Science Ltd. All rights reserved.
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