Macrocyclic Esters1

Spanagel, E. W.; Carothers, W. H.

doi:10.1021/ja01308a046

Cited by 139Chemical Synthesis and ReactionsSupramolecular Chemistry and ComplexesPolymer Synthesis and Characterization

Macrocyclic Esters1

Spanagel, E. W., Carothers, W. H.·1935·Journal of the American Chemical Society

DOI 10.1021/ja01308a046

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ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTMacrocyclic Esters1E. W. Spanagel and W. H. CarothersCite this: J. Am. Chem. Soc. 1935, 57, 5, 929–934Publication Date (Print):May 1, 1935Publication History Published online1 May 2002Published inissue 1 May 1935https://pubs.acs.org/doi/10.1021/ja01308a046https://doi.org/10.1021/ja01308a046research-articleACS PublicationsRequest reuse permissionsArticle Views557Altmetric-Citations125LEARN 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

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Depending on the starting polyesters, either cyclic monomer or dimer were obtained in moderate yield (50-70%) and selectivity (50~90%).
“Depending on the starting polyesters, either cyclic monomer or dimer were obtained in moderate yield (50-70%) and selectivity (50 ~ 90%).”
From Catalysis as an Enabling Science for Sustainable Polymers (2018) · cites this paper as [457]
Back in 1939, Carothers described the selective depolymerization of polydecanoate, polytridecanoate and polytetradecanoate at 270 °C and 1 mm Hg pressure using MgCl2 or SnCl2 as the catalyst.
“Back in 1939, Carothers has described the selective depolymerization of polydecanoate, polytridecanoate and polytetradecanoate at 270 °C and 1 mm Hg pressure using MgCl2 or SnCl2 as the catalyst.456,457”
From Catalysis as an Enabling Science for Sustainable Polymers (2018) · cites this paper as [457]

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Rintoul, W. (1936) · Angewandte Chemie · doi:10.1002/ange.19360490207 · Cited by 4 · see citing works

Authors: Spanagel, E. W., & Carothers, W. H.
Venue: Journal of the American Chemical Society
Publisher: American Chemical Society (ACS)
Published: 1935-05
Volume: 57
Issue: 5
Pages: 929-934
ISSN: 0002-7863 (ISSN-L)
1520-5126
DOI: 10.1021/ja01308a046
OpenAlex: W4234508689
Cited by: 139
References: 0
Citations by year: 2026: 2 · 2025: 6 · 2024: 2 · 2023: 3 · 2022: 1 · 2021: 2 · 2020: 3 · 2019: 3 · 2018: 2 · 2017: 3 · 2016: 6 · 2015: 5 · 2014: 8 · 2013: 5 · 2012: 5
FWCI: 2.36
Type: journal article
Language: en
Open access: closed
Locations: Journal of the American Chemical Society (publishedVersion)
Topics: Physical Sciences › Chemistry › Organic Chemistry › Chemical Synthesis and Reactions
Physical Sciences › Chemistry › Organic Chemistry › Supramolecular Chemistry and Complexes
Physical Sciences › Materials Science › Polymers and Plastics › Polymer Synthesis and Characterization
Keywords: cyclic esters, ester synthesis, ring-closure reactions

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