An approach to bi-tetrahydrofurans from glucose and a correction of the literature
โ Scribed by Alan P. Kozikowski; G.Q. Lin; James P. Springer
- Publisher
- Elsevier Science
- Year
- 1987
- Tongue
- French
- Weight
- 275 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
As part of a class action suit, the author was asked to assess the quality of mental health services in eight prisons in Georgia. This paper describes the background to the suit, reviews selected literature on assessing quality of correctional mental health care, and describes methods used to survey
## Abstract For Abstract see ChemInform Abstract in Full Text.
The bis(tetrahydrofuran) moiety of (+)-asteltoxin which possesses six asymmetric carbons has been synthesized stereoselectively. The synthesis was started from a highly functionalized tetrahydrofuran prepared from P-glucose. (+)-Asteltoxin (L), which was isolated from cultures of AspergiZZus stell
A Ferrier rearrangement and [~-hydroxyketone transposition are key steps in a route to a pancratistatin C-ring precursor. A key feature of the strategy is the pseudoinversion accomplished by ~hydroxyketone transposition, which allows convenient access from methyl (z-D-glucopyranoside. Arylations of
## Abstract Stroke remains an increasing worldwide cause of disability and mortality, and it is the second leading cause of death in industrialized countries.1 Patients with atrial fibrillation form a unique group with increased risk of cardioembolic stroke. Despite the widespread application of th