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Diastereoselective desymmetric 1,2-cis-glycosylation of meso-diols via chirality transfer from a gly...

Diastereoselective desymmetric 1,2-cis-glycosylation of meso-diols via chirality transfer from a gly...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_6a02c12a16984aab9f77d059b704e15f

Diastereoselective desymmetric 1,2-cis-glycosylation of meso-diols via chirality transfer from a glycosyl donor

About this item

Full title

Diastereoselective desymmetric 1,2-cis-glycosylation of meso-diols via chirality transfer from a glycosyl donor

Publisher

London: Nature Publishing Group UK

Journal title

Nature communications, 2020-05, Vol.11 (1), p.2431-2431, Article 2431

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Chemical desymmetrization reactions of
meso
-diols are highly effective for the precise and efficient synthesis of chiral molecules. However, even though enzyme-catalyzed desymmetric glycosylations are frequently found in nature, there is no method for highly diastereoselective desymmetric chemical glycosylation of
meso
-diols. Herein,...

Alternative Titles

Full title

Diastereoselective desymmetric 1,2-cis-glycosylation of meso-diols via chirality transfer from a glycosyl donor

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_6a02c12a16984aab9f77d059b704e15f

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_6a02c12a16984aab9f77d059b704e15f

Other Identifiers

ISSN

2041-1723

E-ISSN

2041-1723

DOI

10.1038/s41467-020-16365-8

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