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...
Autors principals: | Winter, C, Pullin, R, Donohoe, T |
---|---|
Format: | Journal article |
Publicat: |
Elsevier
2017
|
Ítems similars
-
Tethered aminohydroxylation: synthesis of the β-amino acid of microsclerodermins A and B.
per: Pullin, R, et al.
Publicat: (2013) -
DehydromicroscleroderminB and MicroscleroderminJ: Total synthesis and structural revision
per: Melikhova, E, et al.
Publicat: (2016) -
ORGN 482-Studies toward the synthesis of microsclerodermin F
per: Kershaw, J, et al.
Publicat: (2008) -
Studies towards the synthesis of complex amino acids derived from microsclerodermins
per: Rathi, AH
Publicat: (2012) -
Total synthesis and stereochemical reassignment of dehydromicrosclerodermin B and microsclerodermin J
per: Melikhova, E
Publicat: (2016)