New explortion of N-((2S,3R,4R,5R,6R)-2,4,5-Trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)acetamide

Do you like my blog? If you like, you can also browse other articles about this kind. name: N-((2S,3R,4R,5R,6R)-2,4,5-Trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)acetamide. Thanks for taking the time to read the blog about 14215-68-0

In an article, published in an article, once mentioned the application of 14215-68-0, Name is N-((2S,3R,4R,5R,6R)-2,4,5-Trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)acetamide,molecular formula is C8H15NO6, is a conventional compound. this article was the specific content is as follows.name: N-((2S,3R,4R,5R,6R)-2,4,5-Trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)acetamide

2-Acetamido-2-deoxy-l-iminosugar C-Alkyl and C-Aryl Glycosides: Synthesis and Glycosidase Inhibition

The synthesis of a series of six-membered 2-acetamido l-iminosugar C-alkyl and C-aryl glycosides is reported. A diastereoselective sugar-ring enlargement/C-alkylation (or arylation) /ring-contraction sequence applied to d-gluco- and d-manno-configured 2-acetamido azidolactols provides new l-iminosugar C-glycosides. The 1,2-trans stereocontrolled introduction of the pseudoanomeric substituent in these heterocycles strongly suggests a NHAc neighbouring-group participation. In their deprotected form, the nine iminosugars exhibit moderate hexosaminidases and beta-glucuronidase inhibition.

Do you like my blog? If you like, you can also browse other articles about this kind. name: N-((2S,3R,4R,5R,6R)-2,4,5-Trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)acetamide. Thanks for taking the time to read the blog about 14215-68-0

Reference£º
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics