16749-66-9Relevant academic research and scientific papers
The orientation of the β-hydroxyl group controls the diastereoselectivity during the hydride reduction and Grignard reaction of inososes
Jagdhane, Rajendra C.,Patil, Madhuri T.,Krishnaswamy, Shobhana,Shashidhar, Mysore S.
, p. 5144 - 5151 (2013/06/27)
A comparison of the results of the Grignard reaction and the hydride reduction of the carbonyl group of epi- and scyllo-inososes reveals that the extent of diastereoselectivity of these reactions is decided by the orientation of the β-hydroxyl group (or i
Sulfonate protecting groups. Synthesis of O- and C-methylated inositols: D- and L-ononitol, D- and L-laminitol, mytilitol and scyllo-inositol methyl ether
Sarmah, Manash P.,Shashidhar, Mysore S.,Sureshan, Kana M.,Gonnade, Rajesh G.,Bhadbhade, Mohan M.
, p. 4437 - 4446 (2007/10/03)
Syntheses of d- and l-ononitol, d- and l-laminitol, mytilitol and scyllo-inositol methyl ether starting from myo-inositol are described. One or two of the myo-inositol 1,3,5-orthoformate hydroxyl groups were protected as tosylates. These mono or ditosylat
Katalytische, photoinduzierte Charge-Transfer-Osmylierung, ein neuer Weg von Arenen zu Cyclitderivaten
Motherwell, William B.,Williams, Alvin S.
, p. 2207 - 2209 (2007/10/03)
Keywords: Aren-Oxidation; Charge-Transfer; Condurite; Inosite; Osmylierung
Syntheses of Optically Active 2,3,6-Tri-O-benzyl-D-myo-inositol, Laminitol, and Mytilitol from D-Glucose
Sato, Ken-ichi,Bokura, Masayuki,Taniguchi, Makoto
, p. 1633 - 1640 (2007/10/02)
2,3,6-Tri-O-benzyl-D-myo-inositol, which is a key intermediate of D-inositol 1,4,5-triphosphate, was synthesized from D-glucose without performing any optical resolution by utilizing C2 symmetry.Laminitol and mytilitol were also synthesized from D-glucose
