890027-41-5Relevant academic research and scientific papers
Enantioselective total synthesis of (+)-ophiobolin A
Tsuna, Kazuhiro,Noguchi, Naoyoshi,Nakada, Masahisa
supporting information, p. 5476 - 5486 (2013/06/05)
The enantioselective total synthesis of (+)-ophiobolin A is described. This total synthesis features the construction of the spiro CD ring of (+)-ophiobolin A through a stereoselective intramolecular Hosomi-Sakurai cyclization reaction, the joining of the
Research on the pig liver esterase (PLE)-catalyzed kinetic resolution of half-esters derived from prochiral diesters
Noguchi, Naoyoshi,Tsuna, Kazuhiro,Nakada, Masahisa
, p. 357 - 361 (2013/06/27)
The pig liver esterase (PLE)-catalyzed kinetic resolution of half-esters derived from prochiral diesters is described. Generally, the PLE-catalyzed enantioselective hydrolysis of prochiral diesters affords the corresponding half-esters in high yield, beca
Synthetic studies on (+)-ophiobolin A: Asymmetric synthesis of the spirocyclic CD-ring moiety
Noguchi, Naoyoshi,Nakada, Masahisa
, p. 2039 - 2042 (2007/10/03)
Asymmetric synthesis of the spirocyclic CD-ring moiety of (+)-ophiobolin A is described. Fragment A, which was prepared via pig liver esterase (PLE)-mediated kinetic resolution, and fragment B, which was prepared via diastereoselective allylation and subs
