Evidence map›Paper›PMID 34142755›Full record

ReviewChemical record (New York, N.Y.)2021

Glycosyl Sulfonates Beyond Triflates.

Clay S Bennett

Abstract readReview
In one paragraph

Review in Chemical record (New York, N.Y.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author.

Clay S BennettDepartment of Chemistry, Tufts University, 62 Talbot Ave., 02155, Medford, MA, USA.ORCID http://orcid.org/0000-0001-8070-4988

Funding

Reagent Control for Stereoselective Glycosylation ReactionsU01GM120414 · NIGMS · TUFTS UNIVERSITY MEDFORD · PI BENNETT, CLAY SAMUEL · 2016 to 2019
$1.5M
NIGMS NIH HHS U01 GM120414
6 · The paper itself

Abstract

While glycosyl triflates are frequently invoked as intermediates in many chemical glycosylation reactions, the chemistry of other glycosyl sulfonates remains comparatively underexplored. Given the reactivity of sulfonates can span several orders of magnitude, this represents an untapped resource for the development of stereoselective glycosylation reactions. This personal account describes our laboratories efforts to take advantage of this reactivity to develop β-specific glycosylation reactions. Initial investigations led to the development of 2-deoxy-sugar tosylates as highly selective donors for β-glycoside synthesis, an approach which has been used to great success by our group and others for the construction of deoxy-sugar oligosaccharides and natural products. Subsequent studies demonstrate that "matching" the reactivity of the sulfonate to that of the sugar donor leads to highly selective S

Indexed as

OligosaccharidesGlycosylationStereoisomerismOligosaccharidesCarbohydratesGlycosylationNatural ProductsNucleophilic AdditionSynthetic Methods

Identifiers

PMID34142755
PMCPMC10923190

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.