Thiocarbonyl Research Articles

A synthesis of highly hindered thioketones

A synthesis of highly hindered thioketones

Trialkylphosphine-carbon disulphide adducts as reagents for the synthesis of transition metal thiocarbonyl complexes

Die 1:1-molare Umsetzung des Cycloocten- Mn-Komplexes (I) mit dem 1:1-Tricyclohexylphosphin-CS2-Addukt (II) fuhrt hauptsachlich zu dem Phosphin-Substitutionsprodukt (IIIa).

An acidity function based on thiocarbonyl indicators

not available

Use of thionyl chloride for imination of active methylene compounds. Conversion of α-chlorosulfenyl chlorides to imines via thiocarbonyl S-imides

Verbindungen mit aktiven Methylengruppen (I) reagieren mit Thionylchlorid (II) zu den Chlor-sulfenylchloriden (III), die mit den Aminen (IV) zu den Chlor-sulfenamiden (V) substi- tuiert werden.

ChemInform Abstract: EXCITED STATE PROPERTIES OF AROMATIC THIO KETONES‐ THIOFLUORENONE (PART II)

Chemischer InformationsdienstVolume 7, Issue 39 Physical Organic Chemistry ChemInform Abstract: EXCITED STATE PROPERTIES OF AROMATIC THIO KETONES- THIOFLUORENONE (PART II) O. SERAFIMOV, O. SERAFIMOVSearch for more papers by this authorH. J. HAINK, H. J. HAINKSearch for more papers by this authorJ. ROBERT HUBER, J. ROBERT HUBERSearch for more papers by this author O. SERAFIMOV, O. SERAFIMOVSearch for more papers by this authorH. J. HAINK, H. J. HAINKSearch for more papers by this authorJ. ROBERT HUBER, J. ROBERT HUBERSearch for more papers by this author First published: September 28, 1976 https://doi.org/10.1002/chin.197639045AboutPDF 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. Volume7, Issue39September 28, 1976 RelatedInformation

Thiocarbonyl photochemistry .V. Light induced reactions of 3-methyl 4-thiouracil with methacrylonitrile

Thiocarbonyl photochemistry .V. Light induced reactions of 3-methyl 4-thiouracil with methacrylonitrile

Ozonization of Thioketones and Aryl Arenedithiocarboxylates, a Novel Route to Sterically Hindered Sulfines1

Ozonization of Thioketones and Aryl Arenedithiocarboxylates, a Novel Route to Sterically Hindered Sulfines¹

Thiocarbonyl photochemistry. I. Hydroxyalkylation of 1,3-dimethyl 4-thiouracil

1,3-Dimethyl-uracil (I) reagiert bei der Photolyse in Athanol oder Propanol (IIa) und (IIb) zu den Addukten (IIIa) und (IIIb); aus (IV) ist (V) zuganglich, das in (III) ubergeht.

Pyrolysis of 2-azidoaryl thioketones: A novel route to 2,1-benzisothiazoles

Pyrolysis of 2-azidoaryl thioketones: A novel route to 2,1-benzisothiazoles

Reactions of 2,2-Dicyano-3,3-bis(trifluoromethyl)oxirane with Thiocarbonyl Compounds1

Reactions of 2,2-Dicyano-3,3-bis(trifluoromethyl)oxirane with Thiocarbonyl Compounds¹

Sulfines by oxidation of thioketones

Sulfines by oxidation of thioketones

Fluorothiocarbonyl Compounds.1 I. Preparation of Thio Ketones, Thioacyl Halides, and Thio Esters

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTFluorothiocarbonyl Compounds.1 I. Preparation of Thio Ketones, Thioacyl Halides, and Thio EstersW. J. Middleton, E. G. Howard, and W. H. SharkeyCite this: J. Org. Chem. 1965, 30, 5, 1375–1384Publication Date (Print):May 1, 1965Publication History Published online1 May 2002Published inissue 1 May 1965https://doi.org/10.1021/jo01016a008RIGHTS & PERMISSIONSArticle Views696Altmetric-Citations150LEARN 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

Applications of NMR spectroscopy in the field of polycondensed aromatic systems

Abstract Ortho and peri effects due to cyclic heteroatoms and (thio)carbonyl functions have been compared in the (1-thio)chromone and (thio)xanthen-9-one series. As a result of this work, the 7H-benzo[c]thioxanthen-7-one structure XVI has been assigned to the benzothioxanthone first isolated by Davis and Smile, 3 and the 12H-benzo[b]thioxanthen-12-one structure XVII has been assigned to a new compound synthesized as part of this study. IR spectroscopy has been used to provide certain supplementary information

4. Thermochromism of compounds containing the thiocarbonyl and disulphide functions

4. Thermochromism of compounds containing the thiocarbonyl and disulphide functions

176. The constitution and reactions of thiocarbonyl tetrachloride. Part I. Reaction with arylamines

176. The constitution and reactions of thiocarbonyl tetrachloride. Part I. Reaction with arylamines