135943-79-2Relevant academic research and scientific papers
Enantio- and diastereocontrolled total synthesis of (+)-strictifolione
Kumar, Pradeep,Pandey, Menaka,Gupta, Priti,Naidu, S. Vasudeva,Dhavale, Dilip D.
experimental part, p. 6993 - 7004 (2011/02/25)
A concise and practical enantioselective synthesis of (+)-strictifolione has been achieved in high diastereomeric excess using Jacobsen's hydrolytic kinetic resolution, proline-catalyzed sequential α-aminoxylation and Horner-Wadsworth-Emmons olefination o
Total synthesis of (+)-cryptocaryalactone and of a diastereoisomer of (+)-strictifolione via ring-closing metathesis (RCM) and olefin cross-metathesis (CM)
Sabitha, Gowravaram,Vangala, Bhaskar,Reddy, S. Siva Sankara,Yadav, Jhillu S.
experimental part, p. 329 - 338 (2010/05/15)
Ring-closing metathesis (RCM) and olefin cross-metathesis (CM) reactions were used as the key steps for the synthesis of (+)-cryptocaryalactone (1) and the first synthesis of the diastereoisomer 3 of (+)-strictifolione, starting from the commercially avai
Optically Pure 1,3-Diols from (2R,4R)- and (2S,4S)-1,2:4,5-Diepoxypentane
Rychnovsky, Scott D.,Griesgraber, George,Zeller, Sam,Skalitzky, Donald J.
, p. 5161 - 5169 (2007/10/02)
Optically pure (>97percent ee) (2R,4R)-1,2:4,5-diepoxypentane (1) and its enantiomer can be prepared in three steps from 2,4-pentanedione without the need for chromatographic purification.Diepoxide 1 is an efficient precursor to a wide variety of opticall
