213818-71-4Relevant academic research and scientific papers
Stereoselective total synthesis of cephalosporolide D
Shiina, Isamu,Fujisawa, Hidehiko,Ishii, Toshihiro,Fukuda, Yoshio
, p. 1105 - 1123 (2000)
An efficient method for the synthesis of (-)-cephalosporolide D is established via successive enantioselective aldol and effective 8-membered ring lactone forming reactions.
A concise stereoselective total synthesis of (-)-cephalosporolide D
Alluraiah, Gurrala,Sreenivasulu, Reddymasu,Sadanandam, Palle,Anitha, Kowthalam,Raju, Rudraraju Ramesh
, p. 451 - 455 (2016/02/16)
A concise stereoselective total synthesis of eight-membered lactone (-)-cephalosporolide D has been derived from inexpensive and commercially available starting material (S)-propylene epoxide. This concise synthesis utilizes Grignard reaction, Noyori asym
Determination of Relative and Absolute Stereochemistry of Cephalosporolide D and Its Enantioselective Total Synthesis
Shiina, Isamu,Fukuda, Yoshio,Ishii, Toshihiro,Fujisawa, Hidehiko,Mukaiyama, Teruaki
, p. 831 - 832 (2007/10/03)
An efficient method for the synthesis of (-)-cephalosporolide D was established via successive enantioselective aldol reaction and effective construction of 8-membered ring lactone moiety.
