198200-37-2Relevant academic research and scientific papers
Total syntheses of HMP-Y1, hibarimicinone, and HMP-P1
Liau, Brian B.,Milgram, Benjamin C.,Shair, Matthew D.
, p. 16765 - 16772 (2013/01/15)
Total syntheses of HMP-Y1, atrop-HMP-Y1, hibarimicinone, atrop-hibarimicinone, and HMP-P1 are described using a two-directional synthesis strategy. A novel benzyl fluoride Michael-Claisen reaction sequence was developed to construct the complete carbon sk
Diastereoselective hydroboration of substituted exo-glucals revisited. A convenient route for the preparation of L-iduronic acid derivatives
Rochepeau-Jobron, Laurence,Jacquinet, Jean-Claude
, p. 395 - 406 (2007/10/03)
Suitably protected derivatives of methyl 3-O-benzyl-6-deoxy-α-D-xylo- hex-5-enopyranoside, readily prepared from 3-O-benzyl-D-glucopyranose, were reacted with various boranes to prepare the corresponding L-idose components. Reaction of methyl 2-O-benzoyl-3-O-benzyl-6-deoxy-4-O-tert- butyldimethylsilyl-α-D-xylo-hex-5-enopyranoside with 9- borabicyclo[3.3.1]nonane (9-BBN) afforded an easily separable 9:1 L-ido:D- gluco mixture. The L-ido isomer was then transformed in a straightforward manner into suitably protected L-iduronic acid glycosyl donors (chloride, bromide, trichloroacetimidate) which could serve as highly elaborated building blocks in syntheses of L-iduronic acid containing glycosaminoglycan fragments. An unexpected side-reaction occurring in the preparation of 1-O- trichloroacetimidoyl derivatives is also reported.
