428874-41-3Relevant academic research and scientific papers
Enantioselective Total Synthesis of Fluvirucinin B1
Guignard, Guillaume,Llor, Núria,Molins, Elies,Bosch, Joan,Amat, Mercedes
supporting information, p. 1788 - 1791 (2016/05/19)
A convergent synthesis of fluvirucinin B1 from acid ent-6a and nitrile ent-9, involving an organocopper coupling, a stereoselective allylation, a ring-closing metathesis reaction, and a stereoselective hydrogenation as the key steps, is reported. The starting building blocks have been prepared in a straightforward manner from a common phenylglycinol-derived lactam 1. An unprecedented regioselective oxidation of phenylglycinol-derived secondary amines 5 to carboxylic acids 6 has been developed.
A convergent three-component total synthesis of the powerful immunosuppressant (-)-sanglifehrin A
Paquette, Leo A.,Duan, Maosheng,Konetzki, Ingo,Kempmann, Christoph
, p. 4257 - 4270 (2007/10/03)
The potent immunosuppressive agent (-)-sanglifehrin A (5), initially discovered in a soil sample from Malawi, has been synthesized in a highly conver soil gent and stereocontrolled manner. The enantioselective approach relies on initial construction of th
Synthesis of the tripeptide (C1-N12) and hydroxylated hexadecene (C26-C41) domains of sanglifehrin A and C
Paquette, Leo A.,Konetzki, Ingo,Duan, Maosheng
, p. 7441 - 7444 (2007/10/03)
Fully enantio-controlled routes to two major segments of the newly discovered immunosuppressants sanglifehrin A and C are described.
