185681-38-3Relevant academic research and scientific papers
Reductive opening of glycal derived highly functionalized 2,3-epoxy-1-iodides with zinc dust: An efficient method for the synthesis of acyclic long chain polyhydroxylated terminal alkenic alcohols
Reddy, L. Vijaya Raghava,Sagar, Ram,Shaw, Arun K.
, p. 1753 - 1756 (2006)
The synthesis of densely functionalized acyclic long chain terminal alkenic alcohols was achieved by reductive opening of glycal derived 2,3-epoxy-1-iodides, with commercial zinc dust alone in a short reaction time with excellent yields involving a simple
A facile stereoselective synthesis of sphingosine and ceramide
Li, Yun-Long,Wu, Yu-Lin
, p. 2079 - 2082 (2007/10/03)
Flexible syntheses of sphingosine and ceramide were achieved by using D-xylose as the chiral pool and a CuCN-catalyzed allylic alkylation reaction of a dimesylate 8 for chain elongation with concomitant control of an E configuration of the double bond. VCH Verlagsgesellschaft mbH, 1996.
