Enantiospecific Total Synthesis of the Hapalindoles, Fischerindoles, and Welwitindolinones<i>via</i>a Redox Economic Approach
Jeremy M. Richter(Bristol-Myers Squibb (Germany)), Phil S. Baran(Scripps Research Institute), Tomás Llamas(Scripps Research Institute), B.W. Whitefield(Scripps Research Institute), Takeshi Masuda(Scripps Research Institute), Antti Pohjakallio(Scripps Research Institute), Yoshihiro Ishihara(Scripps Research Institute)
Cited by 283
Related Papers
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