93079-23-3Relevant articles and documents
An enantiodivergent synthesis of both (+)- and (-)-disparlure from (R)-2,3-cyclohexylideneglyceraldehyde
Dubey, Akhil Kumar,Chattopadhyay, Angshuman
, p. 1516 - 1521 (2011/12/14)
Reduction of ketone 3 derived from (R)-2,3-cyclohexylideneglyceraldehyde 1 with some common hydrides took place with syn-selectivity. The resulting major product 4a has been exploited as a common chiral template to prepare both enantiomers Ia,b of disparlure.