Synthesis Of Enamides Research Articles

ChemInform Abstract: Synthesis of Enamides and Amides in the Tropane Series and Their Local Anaesthetic Properties.

AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

ChemInform Abstract: Ruthenium Complex‐Catalyzed Addition of N‐Aryl Substituted Amides to Alkynes: Novel Synthesis of Enamides.

AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

Synthesis of enamides and amides in the tropane series and their local anesthetic activity

Synthesis of enamides and amides in the tropane series and their local anesthetic activity

Ruthenium complex-catalysed addition of N-aryl substituted amides to alkynes: novel synthesis of enamides

The addition of N-aryl substituted amides to non-activated terminal alkynes is efficiently promoted by the Ru3(CO)12–PCy3 catalyst system, affording the corresponding linear (E)-enamides in good yields with high regio- and stereo-selectivity.

ChemInform Abstract: A Convenient Synthesis of Enamides and Dienamides by Horner‐Wittig and Wadsworth‐Emmons Reactions.

AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

A convenient synthesis of enamides and dienamides by Horner-Wittig and Wadsworth-Emmons reactions

Various N-acyl-N-alkyl-1-amino-alkenes and −1,3-dienes have been efficiently prepared by reacting aldehydes or ketones 3 with N-alkyl-N-(diphenylphosphinoyl)methyl and −N-(diethoxyphosphoryl)methyl carboxamides 1, 2.

Stereospecific One-pot Synthesis of Enamides and Enimides by the Copper Iodide Promoted Vinylic Substitution

Abstract Enamides and enimides were prepared stereospecifically from vinyl bromides by direct vinylic substitution in the presence of copper salt in aprotic polar solvents.

ChemInform Abstract: Pyridines. Part 15. Synthesis of Enamides by Selective N‐Acylation of Silylated Primary Enamines. Results of the Regioselective Metallation of s‐Collidine, 2,4‐Lutidine and 2,4‐Dimethylquinoline.

AbstractThe anions of the 2‐methylpyridine derivatives (I) react with the nitriles (II) and chlorotrimethylsilane to produce the N‐silylated enamines (III).

Pyridines; XV1. Synthesis of Enamides by SelectiveN-Acylation of Silylated Primary Enamines; Results of the Regioselective Metallation ofs-Collidine, 2,4-Lutidine and 2,4-Dimethylquinoline

Pyridines; XV¹. Synthesis of Enamides by Selective<i>N</i>-Acylation of Silylated Primary Enamines; Results of the Regioselective Metallation of<i>s</i>-Collidine, 2,4-Lutidine and 2,4-Dimethylquinoline

Electroorganic chemistry. 60. Electroorganic synthesis of enamides and enecarbamates and their utilization in organic synthesis

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTElectroorganic chemistry. 60. Electroorganic synthesis of enamides and enecarbamates and their utilization in organic synthesisTatsuya Shono, Yoshihiro Matsumura, Kenji Tsubata, Yoshihiro Sugihara, Shinichiro Yamane, Takenobu Kanazawa, and Takao AokiCite this: J. Am. Chem. Soc. 1982, 104, 24, 6697–6703Publication Date (Print):December 1, 1982Publication History Published online1 May 2002Published inissue 1 December 1982https://doi.org/10.1021/ja00388a037RIGHTS & PERMISSIONSArticle Views2059Altmetric-Citations170LEARN 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 (789 KB) Get e-Alerts Get e-Alerts

ChemInform Abstract: SYNTHESIS OF ENAMIDES AND AMIDES BY HYDROZIRCONATION‐ACYLATION OF SCHIFF BASES

Chemischer InformationsdienstVolume 12, Issue 51 Isocyclic Compounds ChemInform Abstract: SYNTHESIS OF ENAMIDES AND AMIDES BY HYDROZIRCONATION-ACYLATION OF SCHIFF BASES K. S. NG, K. S. NGSearch for more papers by this authorD. E. LAYCOCK, D. E. LAYCOCKSearch for more papers by this authorH. ALPER, H. ALPERSearch for more papers by this author K. S. NG, K. S. NGSearch for more papers by this authorD. E. LAYCOCK, D. E. LAYCOCKSearch for more papers by this authorH. ALPER, H. ALPERSearch for more papers by this author First published: December 22, 1981 https://doi.org/10.1002/chin.198151159AboutPDF 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. Volume12, Issue51December 22, 1981 RelatedInformation

Synthesis of enamides and amides by hydrozirconation-acylation of Schiff bases

Synthesis of enamides and amides by hydrozirconation-acylation of Schiff bases

Dilithiated N-allylcarboxamides. A synthesis of enamides

Dilithiated N-allylcarboxamides. A synthesis of enamides

A simple synthesis of enamides from ketoximes

Ketoximes are converted into enimides [as (III)] in excellent yield by refluxing acetic anhydride in pyridine. Use of alumina chromatography during work-up affords the corresponding enamides [as (II)]. The latter are also prepared by reducing oxime acetates in the presence of acetic anhydride with reagents such as chromium(II). The generality of these reactions is established. Enamides show limited chemical reactivity in comparison with enamines. A particular exception is their efficient α-acetoxylation by reagents such as lead tetra-acetate. Attention is directed to the preparation and use of titanium(III) acetate.

The synthesis of enamides

The synthesis of enamides