950206-49-2Relevant articles and documents
A concise stereoselective total synthesis of (2R,2′R)-threo-(+)- methyl-phenidate via a ring-closing metathesis protocol
Krishna, Palakodety Radha,Lopinti, Krishnarao
, p. 1742 - 1744 (2007/12/31)
In the synthesis of (2R,2′R)-threo-(+)-methylphenidate, a ring-closing metathesis approach was adopted to construct the piperidine ring, while Sharpless asymmetric epoxidation was used for the efficient generation of two contiguous stereocenters. Georg Th