反应条件
1.1: p-toluenesulfonic acid monohydrate / benzene / 3 h / Heating 2.1: Mg / tetrahydrofuran / 1 h / Heating 2.2: tetrahydrofuran / 2 h / Heating 3.1: aq. HCl; acetone / 0.5 h / 20 °C 4.1: acetic acid; pyrrolidine / benzene / 2 h / Heating 5.1: sodium hydride / tetrahydrofuran / 0.58 h 5.2: tetrahydrofuran / 13.5 h 6.1: aq. HCl / 60 h / Heating 7.1: thionyl chloride / 17.5 h 8.1: urea; NaOEt / ethanol / 17 h / Heating 9.1: borane-tetrahydrofuran / tetrahydrofuran / 19 h / Heating View Scheme
参考文献
Shiba, Kazuhiro; Ogawa, Kazuma; Ishiwata, Kiichi; Yajima, Kazuyoshi; Mori, Hirofumi
Bioorganic and Medicinal Chemistry, 2006 , vol. 14, # 8 p. 2620 - 2626