An efficient cross metathesis and Pd-catalyzed allylic rearrangement have been successfully used to construct the northern hemisphere of a cytotoxic marine natural product, palmerolide A
A formal total synthesis of palmerolide A has been accomplished by assembling three fragments by mea...
University of Minnesota Ph.D. dissertation. June 2009. Major: Chemisrty. Advisor: Thomas R. Hoye. 1 ...
- Degradative studies of Palmerolides (Macrocyclic polyketides with anticancer behaviour).- Chiral s...
An efficient cross metathesis and Pd-catalyzed allylic rearrangement have been successfully used to ...
A stereoselective synthesis of the proposed structure of palmerolide C (2), a cytotoxic marine macro...
A stereoselective synthesis of the C1-C18 region of marine natural product palmerolide A from chiral...
A stereoselective synthesis of the C1-C18 region of marine natural product palmerolide A from chiral...
The palmerolides are an emerging class of polyketide natural products isolated from marine organism...
An efficient formal total synthesis of the marine natural product palmerolide A is reported herein, ...
Drug discovery is reliant on new developments in natural product chemistry as well as advances in ch...
Enantioselective formal synthesis of macrolactone palmerolide A, a polyketide marine natural product...
Enantioselective formal synthesis of macrolactone palmerolide A, a polyketide marine natural product...
An enantioselective route to palmerolide A is described. The approach features original syntheses of...
The thesis entitled “Total synthesis of palmerolide A, dihydroconduritols and lentiginosine” is divi...
A formal total synthesis of palmerolide A has been accomplished by assembling three fragments by mea...
A formal total synthesis of palmerolide A has been accomplished by assembling three fragments by mea...
University of Minnesota Ph.D. dissertation. June 2009. Major: Chemisrty. Advisor: Thomas R. Hoye. 1 ...
- Degradative studies of Palmerolides (Macrocyclic polyketides with anticancer behaviour).- Chiral s...
An efficient cross metathesis and Pd-catalyzed allylic rearrangement have been successfully used to ...
A stereoselective synthesis of the proposed structure of palmerolide C (2), a cytotoxic marine macro...
A stereoselective synthesis of the C1-C18 region of marine natural product palmerolide A from chiral...
A stereoselective synthesis of the C1-C18 region of marine natural product palmerolide A from chiral...
The palmerolides are an emerging class of polyketide natural products isolated from marine organism...
An efficient formal total synthesis of the marine natural product palmerolide A is reported herein, ...
Drug discovery is reliant on new developments in natural product chemistry as well as advances in ch...
Enantioselective formal synthesis of macrolactone palmerolide A, a polyketide marine natural product...
Enantioselective formal synthesis of macrolactone palmerolide A, a polyketide marine natural product...
An enantioselective route to palmerolide A is described. The approach features original syntheses of...
The thesis entitled “Total synthesis of palmerolide A, dihydroconduritols and lentiginosine” is divi...
A formal total synthesis of palmerolide A has been accomplished by assembling three fragments by mea...
A formal total synthesis of palmerolide A has been accomplished by assembling three fragments by mea...
University of Minnesota Ph.D. dissertation. June 2009. Major: Chemisrty. Advisor: Thomas R. Hoye. 1 ...
- Degradative studies of Palmerolides (Macrocyclic polyketides with anticancer behaviour).- Chiral s...
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