Van Tamelen Research Articles

Trans-9,10-Dihydronaphthalene, precursor of [10]annulene

In confirmation of the original findings of van Tamelen and Burkoth, and in confutation of the later report of Masamune and Seidner, trans-9,10-dihydronaphthalene is converted on u.v. irradiation at –190° into [10]annulene.

Intermediates in the titanocene-promoted fixation-reduction of molecular nitrogen

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTIntermediates in the titanocene-promoted fixation-reduction of molecular nitrogenEugene E. Van Tamelen, Douglas A. Seeley, Stewart W. Schneller, H. Rudler, and W. CretneyCite this: J. Am. Chem. Soc. 1970, 92, 17, 5251–5253Publication Date (Print):August 1, 1970Publication History Published online1 May 2002Published inissue 1 August 1970https://doi.org/10.1021/ja00720a060RIGHTS & PERMISSIONSArticle Views178Altmetric-Citations18LEARN 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 InReddit PDF (340 KB) Get e-Alerts Get e-Alerts

ChemInform Abstract: SYNTH. DES CECROPIA‐JUVENILHORMONS AUS TRANS,TRANS‐FARNESOL

Chemischer Informationsdienst. Organische ChemieVolume 1, Issue 18 Heterocyclic Compounds ChemInform Abstract: SYNTH. DES CECROPIA-JUVENILHORMONS AUS TRANS,TRANS-FARNESOL E. E. VAN TAMELEN, E. E. VAN TAMELENSearch for more papers by this authorJ. P. MCCORMICK, J. P. MCCORMICKSearch for more papers by this author E. E. VAN TAMELEN, E. E. VAN TAMELENSearch for more papers by this authorJ. P. MCCORMICK, J. P. MCCORMICKSearch for more papers by this author First published: May 5, 1970 https://doi.org/10.1002/chin.197018404Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat No abstract is available for this article. Volume1, Issue18May 5, 1970 RelatedInformation

Biogenetic-type total synthesis of ajmaline

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTBiogenetic-type total synthesis of ajmalineEugene E. Van Tamelen and L. K. OliverCite this: J. Am. Chem. Soc. 1970, 92, 7, 2136–2137Publication Date (Print):April 1, 1970Publication History Published online1 May 2002Published inissue 1 April 1970https://doi.org/10.1021/ja00710a059RIGHTS & PERMISSIONSArticle Views553Altmetric-Citations53LEARN 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 InReddit PDF (241 KB) Get e-Alerts Get e-Alerts

Total synthesis of dl-dihydrocorynantheine

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTTotal synthesis of dl-dihydrocorynantheineEugene E. Van Tamelen and Jackson B. Hester Jr.Cite this: J. Am. Chem. Soc. 1969, 91, 26, 7342–7349Publication Date (Print):December 1, 1969Publication History Published online1 May 2002Published inissue 1 December 1969https://doi.org/10.1021/ja01054a023RIGHTS & PERMISSIONSArticle Views256Altmetric-Citations18LEARN 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 InReddit PDF (1 MB) Get e-Alerts Get e-Alerts

Total syntheses of dl-ajmalicine and emetine

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTTotal syntheses of dl-ajmalicine and emetineEugene E. Van Tamelen, C. Placeway, G. P. Schiemenz, and Ian Gloisby WrightCite this: J. Am. Chem. Soc. 1969, 91, 26, 7359–7371Publication Date (Print):December 1, 1969Publication History Published online1 May 2002Published inissue 1 December 1969https://doi.org/10.1021/ja01054a025RIGHTS & PERMISSIONSArticle Views473Altmetric-Citations44LEARN 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 InReddit PDF (2 MB) Get e-Alerts Get e-Alerts

Conversion of molecular nitrogen to hydrazine

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTConversion of molecular nitrogen to hydrazineEugene E. Van Tamelen, Robert B. Fechter, and Stewart W. SchnellerCite this: J. Am. Chem. Soc. 1969, 91, 25, 7196Publication Date (Print):December 1, 1969Publication History Published online1 May 2002Published inissue 1 December 1969https://doi.org/10.1021/ja01053a054RIGHTS & PERMISSIONSArticle Views249Altmetric-Citations21LEARN 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 InReddit PDF (171 KB) Get e-Alerts Get e-Alerts

Total synthesis of yohimbine.

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTTotal synthesis of yohimbineEugene E. Van Tamelen, Maurice Shamma, Albert W. Burgstahler, Joseph Wolinsky, Rudolph Tamm, and Paul E. AldrichCite this: J. Am. Chem. Soc. 1969, 91, 26, 7315–7333Publication Date (Print):December 1, 1969Publication History Published online1 May 2002Published inissue 1 December 1969https://doi.org/10.1021/ja01054a021RIGHTS & PERMISSIONSArticle Views1162Altmetric-Citations40LEARN 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 InReddit PDF (3 MB) Get e-Alerts Get e-Alerts

Total synthesis of dl-corynantheine

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTTotal synthesis of dl-corynantheineEugene E. Van Tamelen and Ian Gloisby WrightCite this: J. Am. Chem. Soc. 1969, 91, 26, 7349–7359Publication Date (Print):December 1, 1969Publication History Published online1 May 2002Published inissue 1 December 1969https://doi.org/10.1021/ja01054a024RIGHTS & PERMISSIONSArticle Views188Altmetric-Citations17LEARN 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 InReddit PDF (1 MB) Get e-Alerts Get e-Alerts

Biogenetic-type synthesis of lupin alkaloids

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTBiogenetic-type synthesis of lupin alkaloidsEugene E. Van Tamelen and Rodger L. FoltzCite this: J. Am. Chem. Soc. 1969, 91, 26, 7372–7377Publication Date (Print):December 1, 1969Publication History Published online1 May 2002Published inissue 1 December 1969https://doi.org/10.1021/ja01054a026RIGHTS & PERMISSIONSArticle Views335Altmetric-Citations26LEARN 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 InReddit PDF (833 KB) Get e-Alerts Get e-Alerts

Compounds Related to Juvenile Hormone. II2

We recently reported (Braun et al. 1968) 2 convenient synthetic pathways leading to methyl 10,11-epoxy-7-ethyl- 3,11-dimethyl-2,6-tridecadienoate (I) (see Fig. 1), the insect juvenile hormone isolated by Roller et al. (1967) from adult male cecropia moths, Hyalophora cecropia (L.), and later identified by the same group (Dahm et al. 1967). Even though compound I, I-a, when it is prepared by our methods, is presumably a mixture of all 16 possible isomers, it displayed very high juvenile hormone activity when it was assayed with pupae of the yellow mealworm, Tenebrio molitor L., by the method of Bowers and Thompson (1963). Compound I-a was about ⅓ as active as the natural juvenile hormone (Roller et al. 1965) and twice as active as methyl 10,11-epoxy-3,7,11-trimethyl-2,6- dodecadienoate (II) (Bowers et al. 1965), one of the most active synthetic compounds to date. Subsequent preparation of additional quantities of I by reaction scheme B outlined in our earlier publication (Braun et al. 1968) and the more convenient epoxidation procedure using m -chloroperbenzoic acid led to a product (I-b) with activity about ⅓ that of our product (I-a), which was prepared using the epoxidation method of van Tamelen and Sharpless (1967). This loss of activity is not surprising, since peracid epoxidation is known to be much less selective (leading to a mixture of 10,11 and 6,7 epoxides) than the van Tamelen procedure, which yields terminal epoxides almost exclusively.

Compounds Related to Juvenile Hormone. III.2

We recently reported (Braun et al. 1968) 2 convenient synthetic pathways leading to methyl 10,11-epoxy-7-ethyl- 3,11-dimethyl-2,6-tridecadienoate (I) (see Fig. 1), the insect juvenile hormone isolated by Röller et al. (1967) from adult male cecropia moths, Hyalophora cecropia (L.), and later identified by the same group (Dahm et al. 1967). Even though compound I, I-a, when it is prepared by our methods, is presumably a mixture of all 16 possible isomers, it displayed very high juvenile hormone activity when it was assayed with pupae of the yellow mealworm, Tenebrio molitor L., by the method of Bowers and Thompson (1963). Compound I-a was about ⅓ as active as the natural juvenile hormone (Röller et al. 1965) and twice as active as methyl 10,11-epoxy-3,7,11-trimethyl-2,6- dodecadienoate (II) (Bowers et al. 1965), one of the most active synthetic compounds to date. Subsequent preparation of additional quantities of I by reaction scheme B outlined in our earlier publication (Braun et al. 1968) and the more convenient epoxidation procedure using m-chloroperbenzoic acid led to a product (I-b) with activity about ⅓ that of our product (I-a), which was prepared using the epoxidation method of van Tamelen and Sharpless (1967). This loss of activity is not surprising, since peracid epoxidation is known to be much less selective (leading to a mixture of 10,11 and 6,7 epoxides) than the van Tamelen procedure, which yields terminal epoxides almost exclusively.

Photolytic isomerization of aromatic species. Poly-tert-butylfurans

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTPhotolytic isomerization of aromatic species. Poly-tert-butylfuransE. E. Van Tamelen and Thomas H. WhitesidesCite this: J. Am. Chem. Soc. 1968, 90, 14, 3894–3896Publication Date (Print):July 1, 1968Publication History Published online1 May 2002Published inissue 1 July 1968https://doi.org/10.1021/ja01016a071RIGHTS & PERMISSIONSArticle Views79Altmetric-Citations36LEARN 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 InReddit PDF (399 KB) Get e-Alerts Get e-Alerts

Electrolytic reduction of molecular nitrogen

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTElectrolytic reduction of molecular nitrogenEugene E. Van Tamelen and Bjorn AkermarkCite this: J. Am. Chem. Soc. 1968, 90, 16, 4492–4493Publication Date (Print):July 1, 1968Publication History Published online1 May 2002Published inissue 1 July 1968https://doi.org/10.1021/ja01018a074RIGHTS & PERMISSIONSArticle Views405Altmetric-Citations52LEARN 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 InReddit PDF (299 KB) Get e-Alerts Get e-Alerts

An organic-inorganic system for reaction with nitrogen of the air and operation of a facile nitrogen fixation-reduction cycle

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTAn organic-inorganic system for reaction with nitrogen of the air and operation of a facile nitrogen fixation-reduction cycleE. E. van Tamelen, G. Boche, and R. GreeleyCite this: J. Am. Chem. Soc. 1968, 90, 6, 1677–1678Publication Date (Print):March 1, 1968Publication History Published online1 May 2002Published inissue 1 March 1968https://doi.org/10.1021/ja01008a066RIGHTS & PERMISSIONSArticle Views164Altmetric-Citations24LEARN 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 InReddit PDF (273 KB) Get e-Alerts Get e-Alerts

Photolysis of triphenylcarbonium, tropylium, and triphenylcyclopropenium ion

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTPhotolysis of triphenylcarbonium, tropylium, and triphenylcyclopropenium ionEugene E. Van Tamelen, T. M. Cole, R. Greeley, and H. SchumacherCite this: J. Am. Chem. Soc. 1968, 90, 5, 1372–1374Publication Date (Print):February 1, 1968Publication History Published online1 May 2002Published inissue 1 February 1968https://doi.org/10.1021/ja01007a061RIGHTS & PERMISSIONSArticle Views132Altmetric-Citations20LEARN 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 InReddit PDF (395 KB) Get e-Alerts Get e-Alerts

Biosynthesis of fusidic acid from squalene 2,3-oxide

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTBiosynthesis of fusidic acid from squalene 2,3-oxideWagn O. Godtfredsen, Henning O. B. Lorck, Eugene E. Van Tamelen, J. D. Willett, and Raymond B. ClaytonCite this: J. Am. Chem. Soc. 1968, 90, 1, 208–209Publication Date (Print):January 1, 1968Publication History Published online1 May 2002Published inissue 1 January 1968https://doi.org/10.1021/ja01003a036RIGHTS & PERMISSIONSArticle Views204Altmetric-Citations25LEARN 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 InReddit PDF (279 KB) Get e-Alerts Get e-Alerts

The role of substrate structure in the initiation of enzymic cyclization of squalene 2,3-oxide. Studies with 2,3-cis-1'-norsqual ene 2,3-oxide and 2,3-trans-1'-norsqualene 2,3-oxide.

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTRole of substrate structure in the initiation of enzymic cyclization of squalene 2,3-oxide. Studies with 2,3-cis-1'-norsqualene 2,3-oxide and 2,3-trans-1'-norsqualene 2,3-oxideRaymond B. Clayton, Eugene E. Van Tamelen, and Ronn G. NadeauCite this: J. Am. Chem. Soc. 1968, 90, 3, 820–821Publication Date (Print):January 1, 1968Publication History Published online1 May 2002Published inissue 1 January 1968https://doi.org/10.1021/ja01005a065RIGHTS & PERMISSIONSArticle Views33Altmetric-Citations22LEARN 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 InReddit PDF (265 KB) Get e-Alerts Get e-Alerts

Nonaromatization reactions of biocyclo[2.2.0]hexa-2,5-diene

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTNonaromatization reactions of biocyclo[2.2.0]hexa-2,5-dieneEugene E. Van Tamelen and Daniel T. CartyCite this: J. Am. Chem. Soc. 1967, 89, 15, 3922–3923Publication Date (Print):July 1, 1967Publication History Published online1 May 2002Published inissue 1 July 1967https://doi.org/10.1021/ja00991a056RIGHTS & PERMISSIONSArticle Views200Altmetric-Citations33LEARN 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 InReddit PDF (271 KB) Get e-Alerts Get e-Alerts

Biological activities of some terminally modified squalene and squalene 2,3-oxide analogs

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTBiological activities of some terminally modified squalene and squalene 2,3-oxide analogsEugene E. Van Tamelen, K. B. Sharpless, J. D. Willett, Raymond B. Clayton, and Alma L. BurlingameCite this: J. Am. Chem. Soc. 1967, 89, 15, 3920–3922Publication Date (Print):July 1, 1967Publication History Published online1 May 2002Published inissue 1 July 1967https://doi.org/10.1021/ja00991a055RIGHTS & PERMISSIONSArticle Views111Altmetric-Citations12LEARN 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 InReddit PDF (413 KB) Get e-Alerts Get e-Alerts