A short synthetic route to (-)-bulgecinine (1), the amino acid moiety of bulgecins, was established by using 1,3-dipolar cycloaddition of N-benzyl- α-methoxycarbonylmethanimine N-oxide (6) to a chiral allylic alcohol (5) with moderate threo selectivity as the key reaction.
CITATION STYLE
Maeda, M., Okazaki, F., Murayama, M., Tachibana, Y., Aoyagi, Y., & Ohta, A. (1997). Total synthesis of (-)-bulgecinine. Chemical and Pharmaceutical Bulletin, 45(6), 962–965. https://doi.org/10.1248/cpb.45.962
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