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Chemical Communications (Cambridge, England)|March 17, 2005
The first enantioselective total synthesis of the anti-Helicobacter pylori agent (+)-spirolaxine methyl etherJames E Robinson, Margaret A Brimble
Natural Product Reports|July 17, 2020
Molecules derived from the extremes of life: a decade laterZoe E Wilson, Margaret A Brimble
Organic & Biomolecular Chemistry|March 21, 2009
Synthesis of spiroacetal-nucleosides as privileged natural product-like scaffoldsKa Wai Choi, Margaret A Brimble
Organic Letters|September 29, 2012
Total synthesis of 7',8'-dihydroaigialospirolTsz-Ying Yuen, Margaret A Brimble
Organic & Biomolecular Chemistry|August 19, 2007
Synthesis and assignment of the absolute configuration of the anti-Helicobacter pylori agents CJ-12,954 and CJ-13,014Margaret A Brimble, Christina J Bryant
Chemical Communications (Cambridge, England)|February 8, 2007
Synthesis of the spiroacetal-containing anti-Helicobacter pylori agents CJ-12,954 and CJ-13,014Margaret A Brimble, Christina J Bryant
Natural Product Reports|April 21, 2009
Molecules derived from the extremes of lifeZoe E Wilson, Margaret A Brimble
Natural Product Reports|July 27, 2007
Synthesis of macrocyclic shellfish toxins containing spiroimine moietiesPatrick D O'Connor, Margaret A Brimble
Current Opinion in Chemical Biology|January 26, 2019
Natural product derived privileged scaffolds in drug discoveryEmma K Davison, Margaret A Brimble
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