Asymmetric synthesis of cytotoxic sponge metabolites R-strongylodiols A and B and an analogue
The asymmetric synthesis of the marine sponge natural products R-strongylodiols A R-1 and B R-2, using a minimum protection strategy, is described. Two approaches were examined and the Noyori asymmetric reduction of ynones was found to be successful for installing the chirality of the natural produc...
Main Authors: | Kirkham, J, Courtney, T, Lee, V, Baldwin, J |
---|---|
Format: | Journal article |
Language: | English |
Published: |
2005
|
Similar Items
-
Asymmetric synthesis of cytotoxic sponge metabolites R-strongylodiols A and B
by: Kirkham, J, et al.
Published: (2004) -
Total synthesis of cytotoxic sponge alkaloids Motuporamines A and B
by: Baldwin, J, et al.
Published: (1999) -
Biomimetic synthesis of marine sponge metabolite spiculoic acid A and establishment of the absolute configuration of the natural product.
by: Kirkham, J, et al.
Published: (2006) -
Total synthesis of cytotoxic sponge alkaloids hachijodines F and G
by: Goundry, W, et al.
Published: (2002) -
Total synthesis of cytotoxic sponge alkaloids hachijodines F and G
by: Goundry, W, et al.
Published: (2003)