Abstract
A diastereoselective version of Katritzky's method for tertiary amine formation provides an efficient route to the highly selective, non-peptidal, delta opioid agonist (+)-4-[(αR)-α-((2S,5R)-4-allyl-2,5-dimethyl-1-piperazinyl)-3 -hydroxybenzyl]-N,N-diethylbenzamide [(+)-BW373U86], 1. © 1995.
Cite
CITATION STYLE
APA
Bishop, M. J., & McNutt, R. W. (1995). An efficient synthesis of the benzhydrylpiperazine delta opioid agonist (+)-BW373U86. Bioorganic and Medicinal Chemistry Letters, 5(12), 1311–1314. https://doi.org/10.1016/0960-894X(95)00213-D
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