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RETRACTED: Efficient and Reproducible Synthesis of an Fmoc-protected Tn Antigen

2021· preprint· en· 0 citations· W4237457411 on OpenAlex· 10.26434/chemrxiv.14182232.v1

Why is this work in the frame?

A frame that forgets how it found something cannot be audited. These are the routes that admitted this work.

Canadian affiliationAn author listed a Canadian institution. This is the only route the usual frame has.
Canadian funderA Canadian agency funded it. The work may carry no Canadian affiliation at all.

Post-publication record

OpenAlex flags this work as retracted, but it carries no matching Retraction Watch record in this frame.

Machine scores (provisional)

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Opus teacher head0.019
GPT teacher head0.236
Teacher spread
0.217 · how far apart the two teachers sit on this one work
Validation status
score_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Abstract

This preprint is retracted at the authors' request. Since its publication, the authors have become aware that the published synthesis does not provide the title compound, instead generating the characterization-similar glycosyl ester of serine. The authors have submitted a corrected version of this article to ChemRxiv (now posted: 10.26434/chemrxiv-2025-zj3h4) to correct the chemical record and are deeply sorry for any wasted effort this original report might have caused others. The total synthesis of the Thomsen-nouveau (Tn) antigen, a tumour-associated O-linked mucin glycopeptide, was achieved through a concise route. The key glycosylation step proved challenging to reproduce from the literature precedents and was most reliably accomplished using a palladium-catalyzed coupling between the glycosyl donor and Fmoc-functionalized serine acceptor to form the target in moderate yields. This is, to the best of our knowledge, the shortest synthesis reported from galactose for preparing this essential building block for large-scale solid phase peptide synthesis.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

The record

Venue
ChemRxiv
Topic
Carbohydrate Chemistry and Synthesis
Field
Chemistry
Canadian institutions
University of Windsor
Funders
Universities Space Research AssociationNatural Sciences and Engineering Research Council of CanadaMitacsWindsor Cancer Centre Foundation
Keywords
GlycopeptideGlycosylationSerineChemistryCombinatorial chemistryAcceptorBiochemistryPhosphorylationPhysics
Has abstract in OpenAlex
yes