The DOI matches its Crossref record.
Selective carbon-carbon bond formation by cross-coupling of Grignard reagents with organic halides. Catalysis by nickel-phosphine complexes
Abstract
ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTSelective carbon-carbon bond formation by cross-coupling of Grignard reagents with organic halides. Catalysis by nickel-phosphine complexesKohei Tamao, Koji Sumitani, and Makoto KumadaCite this: J. Am. Chem. Soc. 1972, 94, 12, 4374–4376Publication Date (Print):June 1, 1972Publication History Published online1 May 2002Published inissue 1 June 1972https://pubs.acs.org/doi/10.1021/ja00767a075https://doi.org/10.1021/ja00767a075research-articleACS PublicationsRequest reuse permissionsArticle Views16875Altmetric-Citations1098LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-Alertsclose Get e-Alerts
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cited by
Nickel-Catalyzed Cross-Couplings Involving Carbon−Oxygen Bonds
Rosen, B. M., Quasdorf, K. W., Wilson, D. A., Zhang, N., Resmerita, A.-M., Garg, N. K., & Percec, V. (2011) · Chemical Reviews · doi:10.1021/cr100259t · Cited by 1,371
Fortman, G. C., & Nolan, S. P. (2011) · Chemical Society Reviews · doi:10.1039/c1cs15088j · Cited by 1,258
The Mechanisms of the Stille Reaction
Espinet, P., & Echavarren, A. M. (2004) · Angewandte Chemie International Edition · doi:10.1002/anie.200300638 · Cited by 959
Magical Power of Transition Metals: Past, Present, and Future (Nobel Lecture)
Negishi, E. (2011) · Angewandte Chemie International Edition · doi:10.1002/anie.201101380 · Cited by 759
Chain Growth Mechanism for Regioregular Nickel-Initiated Cross-Coupling Polymerizations
Sheina, E. E., Liu, J., Iovu, M. C., Laird, D. W., & McCullough, R. D. (2004) · Macromolecules · doi:10.1021/ma0357063 · Cited by 532
Palladiumkatalysierte Kreuzkupplungen: eine historische Perspektive im Kontext der Nobel‐Preise 2010
Johansson Seechurn, C. C. C., Kitching, M. O., Colacot, T. J., & Snieckus, V. (2012) · Angewandte Chemie · doi:10.1002/ange.201107017 · Cited by 499
Zhang, N., Samanta, S. R., Rosen, B. M., & Percec, V. (2014) · Chemical Reviews · doi:10.1021/cr400689s · Cited by 458
Palladium-Catalyzed Cross-Coupling Reactions: A Powerful Tool for the Synthesis of Agrochemicals
Devendar, P., Qu, R.-Y., Kang, W.-M., He, B., & Yang, G.-F. (2018) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.8b03792 · Cited by 448
The Palladium Catalyzed Nucleophilic Substitution of Aryl Halides by Thiolate Anions
Migita, T., Shimizu, T., Asami, Y., Shiobara, J.-I., Kato, Y., & Kosugi, M. (1980) · Bulletin of the Chemical Society of Japan · doi:10.1246/bcsj.53.1385 · Cited by 411
Mechanistic Aspects of the Palladium‐Catalyzed Suzuki‐Miyaura Cross‐Coupling Reaction
D'Alterio, M. C., Casals‐Cruañas, È., Tzouras, N. V., Talarico, G., Nolan, S. P., & Poater, A. (2021) · Chemistry – A European Journal · doi:10.1002/chem.202101880 · Cited by 281
Functions, Therapeutic Applications, and Synthesis of Retinoids and Carotenoids
Álvarez, R., Vaz, B., Gronemeyer, H., & de Lera, Á. R. (2014) · Chemical Reviews · doi:10.1021/cr400126u · Cited by 260
Schleinitz, J., Langevin, M., Smail, Y., Wehnert, B., Grimaud, L., & Vuilleumier, R. (2022) · Journal of the American Chemical Society · doi:10.1021/jacs.2c05302 · Cited by 88
Metadata
- Authors
- Tamao, K., Sumitani, K., & Kumada, M.
- Venue
- Journal of the American Chemical Society
- Publisher
- American Chemical Society (ACS)
- Published
- 1972-06
- Volume
- 94
- Issue
- 12
- Pages
- 4374-4376
- ISSN
- 0002-7863 (ISSN-L)
- 1520-5126
- OpenAlex
- W2085925544
- Cited by
- 1,291
- References
- 0
- FWCI
- 14.59
- Type
- journal article
- Language
- en
- Open access
- closed
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.