223595-53-7Relevant academic research and scientific papers
Heck arylation of endocyclic enecarbamates with diazonium salts. Improvements and a concise enantioselective synthesis of (-)-codonopsinine.
Severino,Roque D Correia
, p. 3039 - 3042 (2007/10/03)
Total enantioselective synthesis of the natural (-)-codonopsinine was accomplished in seven steps with an overall yield of approximately 16% starting from the five-membered endocyclic enecarbamate 4. The total synthesis features a highly efficient and ste
Heck reaction of endocyclic enecarbemates with diazonium salts. Formal enantioselective syntheses of alkaloids (-)-codonopsine and (-)- codonopsinine, and the synthesis of a new C-aryl azasugar
Oliveira, Denilson F.,Severino, Elias A.,Correia, Carlos Roque D.
, p. 2083 - 2086 (2007/10/03)
Formal total syntheses of the pyrrolidine alkaloids (-)-codonopsine and (-)-codonopsinine, as well as the synthesis of a new C-aryl azasugar were accomplished from a common 5-membered, enantiomerically pure endocyclic enecarbamate. The key step in those s
