A concise total synthesis of (+/-)-1-epiaustraline.
[reaction: see text] A concise total synthesis of 1-epiaustraline 3 is described that utilizes a diastereoselective Birch reduction of an electron-deficient pyrrole and a chelation-controlled vinyl Grignard addition to an aldehyde to introduce the C7 stereocenter. The C1 and C2 stereocenters were se...
Main Authors: | Donohoe, T, Sintim, H |
---|---|
Format: | Journal article |
Jezik: | English |
Izdano: |
2004
|
Podobne knjige/članki
-
A noncarbohydrate based approach to polyhydroxylated pyrrolidizines: total syntheses of the natural products hyacinthacine A1 and 1-epiaustraline.
od: Donohoe, T, et al.
Izdano: (2005) -
A noncarbohydrate based approach to polyhydroxylated pyrrolidizines: total syntheses of the natural products hyacinthacine A1 and 1-epiaustraline.
od: Donohoe, T, et al.
Izdano: (2005) -
A concise and efficient synthesis of (-)-allosamizoline.
od: Donohoe, T, et al.
Izdano: (2007) -
A concise and efficient synthesis of (-)-allosamizoline
od: Donohoe, T, et al.
Izdano: (2007) -
Concise Total Synthesis of (+)-Luteoalbusins A and B
od: Adams, Timothy Cho, et al.
Izdano: (2017)