Facile asymmetric synthesis of the d-myo-inositol derivative from diethyl 2,3-O-isopropylidene-d-tartrate

doi:10.1016/0040-4039(95)02290-2

Paper

Facile asymmetric synthesis of the d-myo-inositol derivative from diethyl 2,3-O-isopropylidene-d-tartrate

Published Feb 5, 1996 · T. Sawada, R. Shirai, S. Iwasaki

Tetrahedron Letters

Q3 SJR score

17

Citations

0

Influential Citations

Full textSemantic Scholar

Abstract

Abstract hidden due to publisher request; this does not indicate any issues with the research. Click the full text link above to read the abstract and view the original source.

Study Snapshot

The study demonstrates a facile asymmetric synthesis of the D-myo-inositol derivative from diethyl 2,3-O-isopropylidene-d-tartrate in 7 steps, providing a key intermediate for the synthesis of various protected D-myo-i

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

Paper

Facile asymmetric synthesis of the d-myo-inositol derivative from diethyl 2,3-O-isopropylidene-d-tartrate

References

Phosphatidylinositol 3‐kinase

Phosphatidylinositol 3kinase plays a key role in signal transduction, playing a role in growth factor-dependent mitogenesis, membrane ruffling, glucose uptake, and vesicular trafficking.

A stereoselective route to enantiomerically pure myo-inositol derivatives starting from D-mannitol

This study developed a stereoselective route to enantiomerically pure myo-inositol derivatives using readily available D-mannitol, a key step in the carbocyclization process.

Stereoselective synthesis of methyl (1R) trans- and (1R) cis-hemicaronaldehydes from natural tartaric acid: Application to the synthesis of s-bioallethrin and deltamethrin insecticides§

This study presents a highly efficient enantioselective synthesis of (1R)-trans- and (1R)-cis-hemicaronaldehydes from natural tartaric acid, which can be applied to the synthesis of s-bioallethrin and deltamethrin

Citations