Organic Sulfur Chemistry Research Articles

Biologically oriented organic sulfur chemistry. IV. Synthesis and properties of 1,2,5-trithiepane, a model for study of sulfide and disulfide moieties in proximity

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTBiologically oriented organic sulfur chemistry. IV. Synthesis and properties of 1,2,5-trithiepane, a model for study of sulfide and disulfide moieties in proximityLamar Field and Charles H. FosterCite this: J. Org. Chem. 1970, 35, 3, 749–752Publication Date (Print):March 1, 1970Publication History Published online1 May 2002Published inissue 1 March 1970https://doi.org/10.1021/jo00828a046RIGHTS & PERMISSIONSArticle Views138Altmetric-Citations29LEARN 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 (608 KB) Get e-Alerts Get e-Alerts

Biologically oriented organic sulfur chemistry. 3. Formation of mercaptals, mercaptoles, an orthothioformate, and thiazolidines for the latentiation of thiols.

Biologically oriented organic sulfur chemistry. 3. Formation of mercaptals, mercaptoles, an orthothioformate, and thiazolidines for the latentiation of thiols.

Additions and Corrections - Organic Sulfur Chemistry. I. The Disulfide-Phosphine Reaction. Desulfurization with Tris(diethylamino)phosphine

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTAdditions and Corrections - Organic Sulfur Chemistry. I. The Disulfide-Phosphine Reaction. Desulfurization with Tris(diethylamino)phosphineDavid Harpp, John Gleason, and James SnyderCite this: J. Am. Chem. Soc. 1969, 91, 17, 4942Publication Date (Print):August 1, 1969Publication History Published online26 April 2004Published inissue 1 August 1969https://doi.org/10.1021/ja01045a600RIGHTS & PERMISSIONSArticle Views43Altmetric-Citations-LEARN 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 (124 KB) Get e-Alerts Get e-Alerts

Biologically oriented organic sulfur chemistry. II. Formation of hemimercaptals or hemimercaptoles as a means of latentiating thiols.

Biologically oriented organic sulfur chemistry. II. Formation of hemimercaptals or hemimercaptoles as a means of latentiating thiols.

Biologically oriented organic sulfur chemistry. I. Reactions of thiols with highly reactive carbonyl compounds

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTBiologically oriented organic sulfur chemistry. I. Reactions of thiols with highly reactive carbonyl compoundsLamar Field and B. J. SweetmanCite this: J. Org. Chem. 1969, 34, 6, 1799–1803Publication Date (Print):June 1, 1969Publication History Published online1 May 2002Published inissue 1 June 1969https://doi.org/10.1021/jo01258a059RIGHTS & PERMISSIONSArticle Views146Altmetric-Citations16LEARN 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 (776 KB) Get e-Alerts Get e-Alerts

Organic sulfur chemistry. I. The disulfide-phosphine reaction. Desulfurization with tris(diethylamino)phosphine

Organic sulfur chemistry. I. The disulfide-phosphine reaction. Desulfurization with tris(diethylamino)phosphine

The Organic Chemistry of Sulfur (Tetracovalent Sulfur Compounds) (Suter, Chester Merle)

The Organic Chemistry of Sulfur (Tetracovalent Sulfur Compounds) (Suter, Chester Merle)

Organic Chemistry of Sulfur: The Organic Chemistry of Sulfur. Tetracovalent Sulfur Compounds . By Chester Merle Suter. 858 pp. 6 × 8½ in. Bound in dark green cloth. New York: John Wiley and Sons, Inc.; London: Chapman and Hall, Ltd. $10.00. 1944.

Organic Chemistry of Sulfur: <i>The Organic Chemistry of Sulfur. Tetracovalent Sulfur Compounds</i> . By Chester Merle Suter. 858 pp. 6 × 8½ in. Bound in dark green cloth. New York: John Wiley and Sons, Inc.; London: Chapman and Hall, Ltd. $10.00. 1944.

Organic Chemistry of Sulfur: The Organic Chemistry of Sulfur. Tetracovalent Sulfur Compounds . By Chester Merle Suter. 858 pp. 6 × 8½ in. Bound in dark green cloth. New York: John Wiley and Sons, Inc.; London: Chapman and Hall, Ltd. $10.00. 1944.

Organic Chemistry of Sulfur: <i>The Organic Chemistry of Sulfur. Tetracovalent Sulfur Compounds</i> . By Chester Merle Suter. 858 pp. 6 × 8½ in. Bound in dark green cloth. New York: John Wiley and Sons, Inc.; London: Chapman and Hall, Ltd. $10.00. 1944.

The progress of organic sulfur chemistry

The progress of organic sulfur chemistry