549513-49-7Relevant academic research and scientific papers
Strategy for Enantio- and Diastereoselective Syntheses of All Possible Stereoisomers of 1,3-Polyol Arrays Based on a Highly Catalyst-Controlled Epoxidation of α,β-Unsaturated Morpholinyl Amides: Application to Natural Product Synthesis
Tosaki, Shin-Ya,Horiuchi, Yoshihiro,Nemoto, Tetsuhiro,Ohshima, Takashi,Shibasaki, Masakatsu
, p. 1527 - 1544 (2007/10/03)
We describe a new strategy for enantio- and diastereoselective syntheses of all possible stereoisomers of 1,3-polyol arrays. This strategy relies on a highly catalyst-controlled epoxidation of α,β-unsaturated morpholinyl amides promoted by the Sm-BINOL-Ph
Enantioselective syntheses of cryptocarya triacetate, Cryptocaryolone, and cryptocaryolone diacetate
Smith, Catherine M.,O'Doherty, George A.
, p. 1959 - 1962 (2007/10/03)
(Matrix presented) The enantioselective syntheses of three natural products from Cryptocarya latifolia have been achieved in 13-15 steps from ethyl sorbate. The route relies upon an enantio- and regioselective Sharpless dihydroxylation and a palladium-cat
