Exploiting the regioselectivity of pyroglutamate alkylations for the synthesis of 6-azabicyclo[3.2.1]octanes and 4-azabicyclo[3.3.0]octanes
作者:Kurt G.R. Masschelein、Christian V. Stevens、Nicolai Dieltiens、Diederica D. Claeys
DOI:10.1016/j.tet.2007.03.084
日期:2007.5
Depending on the N-protecting group of pyroglutamates, the reactivity can be directed to the formation of 6-azabicyclo[3.2.1]octanes or 4-azabicyclo[3.3.0]octanes, which are conformationally restricted glutamate analogues.
取决于焦谷氨酸的N-保护基团,反应性可被导向形成构象受限的谷氨酸类似物的6-氮杂双环[3.2.1]辛烷或4-氮杂双环[3.3.0]辛烷。