Free-radical reactions of 2-t-butyl-1,3-butadiene and 2,3-di-t-butyl-1,3-butadiene
Abstract
ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTFree-Radical Reactions of 2-t-Butyl-1,3-butadiene and 2,3-Di-t-butyl-1,3-butadieneEarl S. Huyser, Frederick W. Siegert, Hans J. W. Sinnige, and Hans WynbergCite this: J. Org. Chem. 1966, 31, 8, 2437–2441Publication Date (Print):August 1, 1966Publication History Published online1 May 2002Published inissue 1 August 1966https://pubs.acs.org/doi/10.1021/jo01346a002https://doi.org/10.1021/jo01346a002research-articleACS PublicationsRequest reuse permissionsArticle Views143Altmetric-Citations2LEARN 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
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The conjugation of double bonds promotes radical addition reactions to both CLA and other conjugated diene-containing species.
“The conjugation of double bonds promotes radical addition reactions to both CLA and other conjugated diene-containing species (8).”
From Conjugated linoleic acid is a preferential substrate for fatty acid nitration (2012) · cites this paper as [8]
Cited by
Sorted by citations
Conjugated linoleic acid is a preferential substrate for fatty acid nitration
Bonacci, G., Baker, P. R. S., Salvatore, S. R., Shores, D., Khoo, N. K. H., Koenitzer, J. R., Vitturi, D. A., Woodcock, S. R., Golin-Bisello, F., Cole, M. P., et al. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.401356 · Cited by 147 · see citing works
Osowska-Pacewocka, K., & ZWIERZAK, A. (1985) · Tetrahedron · doi:10.1016/s0040-4020(01)82369-3 · Cited by 17 · see citing works
Catalytic Hydromagnesiation of 2-Alkylbutadienes
Viktorov, N. B., & Zubritskii, L. M. (2001) · Russian Journal of General Chemistry · doi:10.1023/a:1013906827883 · Cited by 4 · see citing works
Gajda, T., & ZWIERZAK, A. (1985) · Tetrahedron · doi:10.1016/s0040-4020(01)96737-7 · Cited by 3 · see citing works
- Authors
- Huyser, E. S., Siegert, F. W., Sinnige, H. J. W., & Wynberg, H.
- Venue
- The Journal of Organic Chemistry
- Publisher
- American Chemical Society (ACS)
- Published
- 1966-08
- Volume
- 31
- Issue
- 8
- Pages
- 2437-2441
- ISSN
- 0022-3263 (ISSN-L)
- 1520-6904
- OpenAlex
- W2064285310
- Cited by
- 4
- References
- 0
- Citations by year
- 2012: 1
- FWCI
- 0.00
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journal of Organic Chemistry (publishedVersion)
- Topics
- Physical Sciences › Chemistry › Organic Chemistry › Free Radicals and Antioxidants
- Physical Sciences › Chemistry › Organic Chemistry › Radical Photochemical Reactions
- Physical Sciences › Chemistry › Physical and Theoretical Chemistry › Chemical Reactions and Mechanisms
- Keywords
- radical reactions, 1,3-butadiene, tert-butyl substituents, radical reactivity
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