Diastereoselective synthesis of the 5-hydroxy-pyrrolidinone amino acid of the microsclerodermins and model studies for an end-game strategy for microsclerodermin B
The first diastereoselective synthesis of the 5-hydroxy-pyrrolidinone amino acid common to eight members of the microsclerodermin family is presented. Our strategy involves formal hydration of an unsaturated precursor via the use of a two-step hydroxybromination-debromination protocol; this procedur...
Κύριοι συγγραφείς: | Winter, C, Pullin, R, Donohoe, T |
---|---|
Μορφή: | Journal article |
Έκδοση: |
Elsevier
2017
|
Παρόμοια τεκμήρια
-
Tethered aminohydroxylation: synthesis of the β-amino acid of microsclerodermins A and B.
ανά: Pullin, R, κ.ά.
Έκδοση: (2013) -
DehydromicroscleroderminB and MicroscleroderminJ: Total synthesis and structural revision
ανά: Melikhova, E, κ.ά.
Έκδοση: (2016) -
ORGN 482-Studies toward the synthesis of microsclerodermin F
ανά: Kershaw, J, κ.ά.
Έκδοση: (2008) -
Studies towards the synthesis of complex amino acids derived from microsclerodermins
ανά: Rathi, AH
Έκδοση: (2012) -
Total synthesis and stereochemical reassignment of dehydromicrosclerodermin B and microsclerodermin J
ανά: Melikhova, E
Έκδοση: (2016)