前往化源商城

Tetrahedron Letters

Efficient synthesis of β-amino bromides

AS Nagle, RN Salvatore, BD Chong, KW Jung

文献索引:Nagle, Advait S.; Salvatore, Ralph N.; Chong, Byong-Don; Woon Jung, Kyung Tetrahedron Letters, 2000 , vol. 41, # 17 p. 3011 - 3014

全文:HTML全文

被引用次数: 45

摘要

β-Aminoalcohols were smoothly converted to β-amino bromides using thionyl bromide and DMF, which were easily isolated without any further purification. Participation by the β-amino group in brominations not only enhanced reaction rates but also promoted stereo-and regioselectivities.