Total synthesis of marine natural products without using protecting groups
Phil S. Baran(Scripps Research Institute), Jeremy M. Richter(Scripps Research Institute), Thomas J. Maimone(University of California, Berkeley)
Cited by 509
Related Papers
Enantiospecific Total Synthesis of the Hapalindoles, Fischerindoles, and Welwitindolinones<i>via</i>a Redox Economic Approach
|Journal of the American Chemical Society|2008|283
Enantioselective Total Syntheses of Welwitindolinone A and Fischerindoles I and G
|Journal of the American Chemical Society|2005|273
Direct Coupling of Indoles with Carbonyl Compounds: Short, Enantioselective, Gram-Scale Synthetic Entry into the Hapalindole and Fischerindole Alkaloid Families
|Journal of the American Chemical Society|2004|249
1,3-Diol Synthesis via Controlled, Radical-Mediated C−H Functionalization
|Journal of the American Chemical Society|2008|233
Scope and Mechanism of Direct Indole and Pyrrole Couplings Adjacent to Carbonyl Compounds: Total Synthesis of Acremoauxin A and Oxazinin 3
|Journal of the American Chemical Society|2007|189