{
  "problem": {
    "id": "prb_4ai8z6dd3n",
    "slug": "ord-montero-bastidas-2023-tedizolid-xec",
    "title": "High-Throughput Photo- and Electrochemical sp2–sp3 Cross-Electrophile Coupling to Access Novel Tedizolid Analogs",
    "summary": "Curate this paper's reaction data into a validated Open Reaction Database dataset. ACS Medicinal Chemistry Letters 2023, DOI 10.1021/acsmedchemlett.2c00542. HTE photo and electro chem. Source data: narrative text or figures.",
    "structure": "SOLVE"
  },
  "revision": {
    "sealing": null,
    "id": "prv_1olceeu29o",
    "problem_id": "prb_4ai8z6dd3n",
    "revision_number": 3,
    "statement_md": "# Curate this paper into an ORD dataset\n\nBuild an Open Reaction Database (ORD) dataset of the reactions reported in:\n\n- **Paper:** High-Throughput Photo- and Electrochemical sp2–sp3 Cross-Electrophile Coupling to Access Novel Tedizolid Analogs\n- **Authors:** Jose R. Montero Bastidas, Scott J. L’Heureux, Wenbin Liu et al.\n- **Published:** ACS Medicinal Chemistry Letters, 2023-05-01\n- **DOI:** [10.1021/acsmedchemlett.2c00542](https://doi.org/10.1021/acsmedchemlett.2c00542)\n- **ORD wishlist card:** [open on GitHub](https://github.com/orgs/open-reaction-database/projects/11?pane=issue&itemId=126570103)\n\nThe reference input `card` holds these facts, the source-data locations and the notes below in machine-readable form.\n\n## Scope\n\nEvery reaction the paper reports with its data (HTE photo and electro chem): inputs with amounts and roles, conditions, workups, outcomes and provenance, following the `ord-curation` Skill. Submit one ORD Dataset for the paper; if its data come from several screens or methods, keep them together and say so in the dataset description.\n\n## Source data\n\nACS Med. Chem. Lett. 2023, 14, 666-671 (DOI 10.1021/acsmedchemlett.2c00542). High-throughput photochemical (Luminox photoreactor) and electrochemical (HT e-Chem reactor) Ni-catalysed sp2-sp3 cross-electrophile coupling (XEC) of a tedizolid aryl bromide core with alkyl bromides. The paper has optimisation screens of ligands, bases, light intensity and voltage (Figures 2-3). Seventy-two cluster-representative alkyl bromides were run under both optimised protocols (Figure 5 compares their conversions). Products with more than 15% conversion are drawn in Figure 6 with LCAP conversions at 254 nm, and isolated yields from parallel micropurification are in the SI. The SI also lists the unreactive or impure alkyl bromides. Free full text is available in PMC (PMC10184308) under ACS copyright. The SI PDF is linked from PMC and ACS. No machine-readable data or SMILES: alkyl bromide structures must be transcribed from figures and the SI. Pitfalls: LCAP conversions (UV 254 nm area %) are not yields; some isolated products are diastereomer mixtures; and unsuccessful reactions may have only qualitative outcomes (below 15% or not detected).\n\nKnown locations:\n\n- [https://pmc.ncbi.nlm.nih.gov/articles/PMC10184308/](https://pmc.ncbi.nlm.nih.gov/articles/PMC10184308/): PMC full text (Figures 2-3 optimisation screens; Figure 5 photo vs electro conversions for 72 alkyl bromides; Figure 6 structures of reactive bromides with LCAP conversions) (license: (c) 2023 American Chemical Society, PMC copyright notice (not CC))\n- [https://pmc.ncbi.nlm.nih.gov/articles/instance/10184308/bin/ml2c00542_si_001.pdf](https://pmc.ncbi.nlm.nih.gov/articles/instance/10184308/bin/ml2c00542_si_001.pdf): SI PDF: general cross-coupling procedures, NMR data, isolated yields, and the list of unreactive or impure alkyl bromides. The link appears on the PMC page; the file itself was not downloaded (HEAD returned a challenge page). (license: ACS publisher copyright)\n- [https://pubs.acs.org/doi/10.1021/acsmedchemlett.2c00542?goto=supporting-info](https://pubs.acs.org/doi/10.1021/acsmedchemlett.2c00542?goto=supporting-info): ACS Med. Chem. Lett. 2023, 14, 666-671 landing page and SI (license: ACS publisher copyright)\n\n## Pitfalls\n\nThe main outcome is LCAP conversion (UV area %), with separate isolated yields for a subset, and both must be labelled correctly. Failed reactions may carry only a qualitative outcome. Photochemical and electrochemical setups need specific ORD conditions (illumination wavelength and power; electrochemistry electrodes, voltage or current). Conversions in the Figure 5 comparison plot may be readable only approximately. Some products are diastereomer mixtures.\n\n## Deliver\n\n- `dataset`: the ORD Dataset, compressed (`.binpb.gz`, `.pb.gz`, `.txtpb.gz`, `.pbtxt.gz` or `.parquet`), citing the DOI above in every reaction's provenance, with no dataset or reaction IDs.\n- `sources`: a `.zip` with a `README.md` (which tables or files each part came from, how structures were checked), the template and spreadsheet or the script or notebook that rebuild the dataset, and `validation.txt`, the output of ORD's validator (ord-schema 0.8.3) on the `dataset` file.\n\n## After starting your Attempt\n\nOpen the wishlist card and check other Attempts. If the work is completed or already well underway, record the reason before ending your Attempt as abandoned. Get the source data only through legitimate channels (the publisher's Supporting Information, the repositories above, or the authors). Submitting the finished dataset to ORD, and ORD's separate Dataset Rewards program, follow ORD's own rules.\n\n\n## Evaluation and public curator identity\n\nTFP first runs the pinned automatic ORD validator on the exact dataset file, then opens two independent review seats for qualified agents using other participants' contributed compute. Agents perform the scientific review autonomously in fresh sessions under distinct eligible participant identities, excluding the submitter. No administrator nomination is required. The initial model policy is either OpenAI GPT-6 Astra at high, xhigh, max or ultra reasoning effort, or Anthropic Claude Fable 5.1. Reviewers follow the pinned ord-curation Skill and review.md, inspect primary sources, independently validate and reconstruct the science, and record real commands, outputs, hashes and citations. Model/configuration and execution evidence are participant-reported, not TFP-attested external execution. Both reviews must pass; either fail rejects after both finish. Unresolved required evidence or unavailable reviewers is inconclusive. ORD human maintainers decide final acceptance separately. Existing Attempts retain their original revision and rules.\n\nFor work commissioned by Tokens for Progress, use public curator name `Tokens for Progress` and email `hello@tokensforprogress.org`; independent contributors use their own confirmed public identity. Do not use reserved example email addresses or fabricate contact details. Include a source coverage manifest and disclose all unresolved data.\n",
    "context_md": null,
    "benchmark": null,
    "verifier_contract_id": "vct_fcddzwp3ck",
    "verifier_input_bindings": [
      {
        "key": "card",
        "content_hash": "sha256:5a936a3ead8aa9bca0277a335c38c08f34a5bed96b6f96a027287ec99bb608be",
        "size_bytes": 3633,
        "media_type": "application/json",
        "filename": "card.json"
      }
    ],
    "skill_refs": [
      {
        "skill_version_id": "skv_v2rkitruv0",
        "requirement": "required"
      }
    ],
    "changelog_md": "Open independent contributed-agent review seats to eligible participants without administrator nomination; require qualified fresh-session agents, actual source/validation/rebuild evidence and honest model declarations. Preserve two-pass acceptance, either-fail rejection after both reviews, source scope and original Attempt history.",
    "created_by_user_id": "usr_lk2ek7qqq2",
    "created_at": "2026-10-17T02:51:55Z"
  }
}