The DOI matches its Crossref record; 9 of the 9 references it cites were found in a registry or an index.
The invention of new radical chain reactions. Part VIII. Radical chemistry of thiohydroxamic esters; A new method for the generation of carbon radicals from carboxylic acids
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Citations
Cites
Two-dimensional spectroscopy. Application to nuclear magnetic resonance
Aue, W. P., Bartholdi, E., & Ernst, R. R. (1976) · The Journal of Chemical Physics · doi:10.1063/1.432450 · Cited by 3,082
A new method for the deoxygenation of secondary alcohols
Barton, D. H. R., & McCombie, S. W. (1975) · Journal of the Chemical Society, Perkin Transactions 1 · doi:10.1039/p19750001574 · Cited by 1,652
Self-citation4‐Dialkylaminopyridines as Highly Active Acylation Catalysts. [New synthetic method (25)]
Höfle, G., Steglich, W., & Vorbrüggen, H. (1978) · Angewandte Chemie International Edition in English · doi:10.1002/anie.197805691 · Cited by 1,203
Recent developments in the carbodiimide chemistry
Mikoz.xl;lajczyk, M., & Kiez.xl;lbasiński, P. (1981) · Tetrahedron · doi:10.1016/s0040-4020(01)92010-1 · Cited by 240
Shaw, E. N., Bernstein, J., Losee, K. A., & Lott, W. A. (1950) · Journal of the American Chemical Society · doi:10.1021/ja01166a008 · Cited by 144
Pfenninger, J., Heuberger, C., & Graf, W. (1980) · Helvetica Chimica Acta · doi:10.1002/hlca.19800630823 · Cited by 113
Radical-Induced Deoxygenation of Primary Alcohols
Barton, D. H. R., Motherwell, W. B., & Stange, A. F. (1981) · Synthesis · doi:10.1055/s-1981-29587 · Cited by 109
Self-citationRadical deoxygenation of tertiary alcohols
Barton, D. H. R., HARTWIG, W., Motherwell, R. S. H., Motherwell, W. B., & Stange, A. F. (1982) · Tetrahedron Letters · doi:10.1016/s0040-4039(00)87249-4 · Cited by 63
Self-citationBarker, P. J., & Backwith, A. L. J. (1984) · Journal of the Chemical Society Chemical Communications · doi:10.1039/c39840000683 · Cited by 33
Cited by
Thiyl Radicals in Organic Synthesis
Dénès, F., Pichowicz, M., Povie, G., & Renaud, P. (2014) · Chemical Reviews · doi:10.1021/cr400441m · Cited by 985
Competition Methods and Scales for Alkyl Radical Reaction Kinetics
Newcomb, M. (1993) · Tetrahedron · doi:10.1016/s0040-4020(01)85808-7 · Cited by 614
The Asymmetric Total Synthesis of (+)- and (−)-Spirotryprostatin B
Sebahar, P. R., & Williams, R. M. (2000) · Journal of the American Chemical Society · doi:10.1021/ja001133n · Cited by 434
Acyclic stereochemical control in free-radical reactions
Porter, N. A., Giese, B., & Curran, D. P. (1991) · Accounts of Chemical Research · doi:10.1021/ar00010a003 · Cited by 373
Radiosynthesis of 11C-Levetiracetam: A Potential Marker for PET Imaging of SV2A Expression
Cai, H., Mangner, T. J., Muzik, O., Wang, M.-W., Chugani, D. C., & Chugani, H. T. (2014) · ACS Medicinal Chemistry Letters · doi:10.1021/ml500285t · Cited by 58
Metadata
- Authors
- Barton, D. H. R., Crich, D., & Motherwell, W. B.
- Venue
- Tetrahedron
- Publisher
- Elsevier BV
- Published
- 1985-01
- Volume
- 41
- Issue
- 19
- Pages
- 3901-3924
- ISSN
- 0040-4020 (ISSN-L)
- OpenAlex
- W2057479286
- Cited by
- 537
- References
- 9
- FWCI
- 10.23
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: The invention of new radical chain reactions. Part VIII. Radical chemistry of thiohydroxamic esters; A new method for the generation of carbon radicals from carboxylic acids. https://app.cochat.ai/papers/10.1016/s0040-4020(01)97173-x
- The paper
- Barton, D. H. R., Crich, D., & Motherwell, W. B. (1985). The invention of new radical chain reactions. Part VIII. Radical chemistry of thiohydroxamic esters; A new method for the generation of carbon radicals from carboxylic acids. Tetrahedron. https://doi.org/10.1016/s0040-4020(01)97173-x
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.
