Evidence map›Paper›PMID 40533722›Full record

ArticleAngewandte Chemie (International ed. in English)2025

Automated Iterative N─C and C─C Bond Formation.

Theodore Tyrikos-Ergas, Sevasti Agiakloglou, Antonio J LaPorte, Wesley Wang, Chieh-Kai Chan, Clare E Wells, Christopher K Rakowski, Rachel I Hammond, Jia Qiu, Jonathan D Raymond and 5 more

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Automated Iterative N─C and C─C Bond Formation.Angewandte Chemie (International ed. in English) · 2025
    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

15 authors.

Theodore Tyrikos-Ergas *Department of Chemistry, University of Illinois, Urbana, IL, 61820, USA.ORCID https://orcid.org/0000-0001-7214-0924
Sevasti Agiakloglou *Department of Chemistry, University of Illinois, Urbana, IL, 61820, USA.ORCID https://orcid.org/0009-0008-6064-1164
Antonio J LaPorteDepartment of Chemistry, University of Illinois, Urbana, IL, 61820, USA.ORCID https://orcid.org/0000-0003-1899-6013
Wesley WangDepartment of Chemistry, University of Illinois, Urbana, IL, 61820, USA.
Chieh-Kai ChanDepartment of Chemistry, University of Illinois, Urbana, IL, 61820, USA.
Clare E WellsDepartment of Chemistry, University of Illinois, Urbana, IL, 61820, USA.
Christopher K RakowskiDepartment of Chemistry, University of Illinois, Urbana, IL, 61820, USA.
Rachel I HammondDepartment of Chemistry, University of Illinois, Urbana, IL, 61820, USA.
Jia QiuDepartment of Chemistry, University of Illinois, Urbana, IL, 61820, USA.
Jonathan D RaymondDepartment of Chemistry, University of Illinois, Urbana, IL, 61820, USA.
Tiago VieiraDeerfield Discovery & Development LLC, a subsidiary of Deerfield Management Company, 345 Park Ave S, New York, NY, 10010, USA.
John LimantoDeerfield Discovery & Development LLC, a subsidiary of Deerfield Management Company, 345 Park Ave S, New York, NY, 10010, USA.
Marc N FeiglinDeerfield Discovery & Development LLC, a subsidiary of Deerfield Management Company, 345 Park Ave S, New York, NY, 10010, USA.
Daniel J BlairDepartment of Chemical Biology & Therapeutics, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
Martin D BurkeDepartment of Chemistry, University of Illinois, Urbana, IL, 61820, USA.ORCID https://orcid.org/0000-0001-7963-7140

Funding

NIH HHS R35118185NSF: Molecule Maker Lab Institute 2019897
6 · The paper itself

Abstract

Small molecule solutions to many contemporary societal challenges await discovery, but the artisanal and manual process via which this class of chemical matter is typically accessed limits the discovery of new functions. Automated assembly of (N-methyl iminodiacetic acid) MIDA or (tetramethyl N-methyl iminodiacetic acid) TIDA boronate building blocks via iterative C─C bond formation, an approach we call "block chemistry", alternatively enables generalized and automated preparation of many different types of small molecules in a modular fashion. But in its current form, this engine cannot also leverage nitrogen atoms as iteration handles. Here, we disclose a new iteration-enabling group, CbzT (p-TIDA boronate-substituted carboxybenzyl), that reversibly attenuates the reactivity of nitrogen atoms and enables generalized catch-and-release purification. CbzT is leveraged to achieve the automated modular synthesis of Imatinib (Gleevec), an archetypical clinically approved kinase inhibitor, in which building blocks are iteratively linked by both N─C and C─C bonds. This work substantially expands the types of small molecules that can be iteratively assembled in an automated modular fashion. It also advances the concept of intentionally developing chemistry that machines can do.

Indexed as

AutomationBlock chemistryBoronatesCbzTIDANitrogen iteration handle

Identifiers

PMID40533722
PMCPMC12338424

What OpenQuestion holds

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LicenceCC BY-NC
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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.