867357-61-7Relevant academic research and scientific papers
(R)-2,3-Cyclohexylideneglyceraldehyde: a novel template for simple entry into both cis- and trans-2,5-disubstituted tetrahydrofurans
Chattopadhyay, Angshuman,Vichare, Prasad,Dhotare, Bhaskar
, p. 2871 - 2873 (2007/10/03)
Sharpless asymmetric dihydroxylation at the terminal olefin of benzoates 3a and 3b, using both AD-mix α and AD-mix β afforded only one diastereomer of diols 5a and 5b, respectively. Diols 5a and 5b were easily transformed into cis- and trans-2,5-disubstit
[3 + 2]-Annulation reactions of chiral allylsilanes and chiral aldehydes. Studies on the synthesis of bis-tetrahydrofuran substructures of annonaceous acetogenins
Mertz, Eric,Tinsley, Jennifer M.,Roush, William R.
, p. 8035 - 8046 (2007/10/03)
Double asymmetric [3 + 2]-annulation reactions of chiral β-silyloxylallylsilanes with chiral 2-tetrahydrofuranyl carboxaldehydes have been studied, leading to the stereocontrolled synthesis of six diastereomeric bis-tetrahydrofuran structures correspondin
