Enantioselective synthesis and absolute configuration of (−)-1-(benzofuran-2-yl)-2-propylaminopentane,((−)-BPAP), a highly potent and selective catecholaminergic …
…, T Yasusa, T Ando, M Watanabe, F Yoneda…
Index: Oka, Takahiro; Yasusa, Takuya; Ando, Takashi; Watanabe, Mayumi; Yoneda, Fumio; Ishida, Toshimasa; Knoll, Joseph Bioorganic and Medicinal Chemistry, 2001 , vol. 9, # 5 p. 1213 - 1219
Full Text: HTML
Citation Number: 24
Abstract
Enantioselective synthesis and absolute configuration of (−)-1-(benzofuran-2-yl)-2- propylaminopentane ((−)-BPAP), which is a highly potent and selective catecholaminergic activity enhancer (CAE) substance, are described. The synthetic approach consists of the coupling reaction of benzofuran with (R)-N-tosyl-2-propylazirizine or (R)-N-methoxy-N- methylnorvaliamide, followed by appropriate modifications of the resulting coupling ...
Related Articles:
[Kim, Haejin; Rhee, Young Ho Journal of the American Chemical Society, 2012 , vol. 134, # 9 p. 4011 - 4014]
Absolute configuration of insect-produced epilachnene
[Farmer, Jay J.; Attygalle, Athula B.; Smedley, Scott R.; Eisner, Thomas; Meinwald, Jerrold Tetrahedron Letters, 1997 , vol. 38, # 16 p. 2787 - 2790]