262853-75-8Relevant academic research and scientific papers
Stannylfuranones in synthesis: Highly enantioselective preparation of (+)-hamabiwalactone B
Richecur, Alexandre M.E.,Sweeney
, p. 8901 - 8904 (1998)
An unambiguous and highly enantioselective total synthesis of the naturally-occurring 2(5H)-furanone hamabiwalactone B has been achieved. The key step is a Stille coupling of novel stannylfuranone 2 with (E)-iodoalkene 3. The enantiomeric purity of the synthetic natural product was ≥ 99%, as judged by chiral HPLC.
Preparation of (+)-Hamabiwalactone B via Stille coupling of an enantiomerically pure stannylfuranone
Richec?ur, Alexandre M. E.,Sweeney
, p. 389 - 395 (2007/10/03)
An unambiguous and highly enantioselective total synthesis of the naturally occurring 2(5H)-furanone Hamabiwalactone B has been achieved. The key step was a palladium-catalysed cross coupling ('Stille' coupling) of the previously unreported stannylfuranone 2 with (E)-iodoalkene 3. The enantiomeric purity of the synthetic natural product was ≥99%, as judged by chiral HPLC. (C) 2000 Elsevier Science Ltd.
