Iwashima, Makoto’s team published research in Tetrahedron Letters in 1995-03-27 | 112-63-0

Tetrahedron Letters published new progress about Alditols Role: SPN (Synthetic Preparation), PREP (Preparation). 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, Application of C19H34O2.

Iwashima, Makoto; Kinsho, Takeshi; Smith, Amos B. III published the artcile< A caveat on the Sharpless asymmetric dihydroxylation>, Application of C19H34O2, the main research area is vinyl C glycoside stereoselective dihydroxylation; alditol; Sharpless stereoselective hydroxylation olefin sugar.

Sharpless asym. dihydroxylation (AD) of the homochiral synthetic intermediates 2a-c gave anomalous results: pairs of pseudoenantiomeric reagents, expected to generate complementary diastereomer ratios characteristic of double diastereoselection, instead generally furnished indistinguishable product mixtures AD reactions of related monosubstituted olefins failed to pinpoint the structural features responsible for the unexpected behavior.

Tetrahedron Letters published new progress about Alditols Role: SPN (Synthetic Preparation), PREP (Preparation). 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, Application of C19H34O2.

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics