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1ChemInform Abstract: CARBON-13 NMR SPECTROSCOPY. XV. CARBON-13 AND PROTON NMR STUDIES ON THE CONFIGURATION OF TRICARBONYLIRON COMPLEXES OF OXA- AND AZA(4.4.3)PROPELLANES

K. Bachmann,Wolfgang von Philipsborn,C. Amith,David Ginsburg

Chemischer InformationsdienstVolume 8, Issue 31 Physical Organic Chemistry ChemInform Abstract: CARBON-13 NMR SPECTROSCOPY. XV. CARBON-13 AND PROTON NMR STUDIES ON THE CONFIGURATION OF TRICARBONYLIRON COMPLEXES OF OXA- AND AZA(4.4.3)PROPELLANES K. BACHMANN, K. BACHMANNSearch for more papers by this authorW. VON PHILIPSBORN, W. VON PHILIPSBORNSearch for more papers by this authorC. AMITH, C. AMITHSearch for more papers by this authorD. GINSBURG, D. GINSBURGSearch for more papers by this author K. BACHMANN, K. BACHMANNSearch for more papers by this authorW. VON PHILIPSBORN, W. VON PHILIPSBORNSearch for more papers by this authorC. AMITH, C. AMITHSearch for more papers by this authorD. GINSBURG, D. GINSBURGSearch for more papers by this author First published: August 2, 1977 https://doi.org/10.1002/chin.197731052AboutPDF 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. Volume8, Issue31August 2, 1977 RelatedInformation

1977Chemischer Informationsdienst（1977）

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2Propellanes—XXXIII

C AMITH,M HACKMEYER,D GINSBURG

Eu(DPM)3 has been used as a shift reagent in studying the NMR spectra of various propellanes. The PDIGM program has been used to calculate the preferred conformations of these substrates.

1976TETRAHEDRON引用：10

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3ChemInform Abstract: PROPELLANES. XXXIII. CONFORMATIONS OF VARIOUS HETEROCYCLIC PROPELLANES

C. AMITH,M. HACKMEYER,D. GINSBURG

Chemischer InformationsdienstVolume 7, Issue 32 Physical Organic Chemistry ChemInform Abstract: PROPELLANES. XXXIII. CONFORMATIONS OF VARIOUS HETEROCYCLIC PROPELLANES C. AMITH, C. AMITHSearch for more papers by this authorM. HACKMEYER, M. HACKMEYERSearch for more papers by this authorD. GINSBURG, D. GINSBURGSearch for more papers by this author C. AMITH, C. AMITHSearch for more papers by this authorM. HACKMEYER, M. HACKMEYERSearch for more papers by this authorD. GINSBURG, D. GINSBURGSearch for more papers by this author First published: August 10, 1976 https://doi.org/10.1002/chin.197632057Read 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 onFacebookTwitterLinkedInRedditWechat No abstract is available for this article. Volume7, Issue32August 10, 1976 RelatedInformation

1976Chemischer Informationsdienst

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4Selective Reduction of 12-Oxa[4.4.3]propella-2,4,7,9-tetraene Catalyzed by an Arenechromium Tricarbonyl

C AMITH,M CAIS,D FRAENKEL,D GINSBURG

AbstractDie Hydrierung des Oxa‐propellatetraens (I) in Gegenwart von Phenanthrentricarbonylchrom (II) liefert die Hydrierungsprodukte (III) und (IV), deren Konformere ausführlich diskutiert werden.

1975HETEROCYCLES（1975）引用：13

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5ChemInform Abstract: PROPELLANES PART 27, REACTIONS OF 4‐PHENYL‐1,2,4‐TRIAZOLINE‐3,5‐DIONE WITH SOME (4,4,3)PROPELLANE ETHERS, IMIDES AND THEIR IRONTRICARBONYL DERIVATIVES

C. AMITH,D. GINSBURG

Chemischer InformationsdienstVolume 5, Issue 51 Heterocyclic Compounds ChemInform Abstract: PROPELLANES PART 27, REACTIONS OF 4-PHENYL-1,2,4-TRIAZOLINE-3,5-DIONE WITH SOME (4,4,3)PROPELLANE ETHERS, IMIDES AND THEIR IRONTRICARBONYL DERIVATIVES C. AMITH, C. AMITHSearch for more papers by this authorD. GINSBURG, D. GINSBURGSearch for more papers by this author C. AMITH, C. AMITHSearch for more papers by this authorD. GINSBURG, D. GINSBURGSearch for more papers by this author First published: December 24, 1974 https://doi.org/10.1002/chin.197451323AboutPDF 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. Volume5, Issue51December 24, 1974 RelatedInformation

1974Chemischer Informationsdienst

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6Propellanes .27. Reactions of "4-Phenyl-1,2,4-triazoline-3,5-dione with Some [4 4 3]propellane Ethers, Imides and Their Irontricarbonyl Derivatives

C AMITH,D GINSBURG

The steric course of Diels-Alder reactions of propellane ethers and methylimides, at different oxidation levels, was investigated. Irontricarbonyl derivatives, particularly of the imides, were subjected to reaction with a potent dienophile and the results are described.

1974TETRAHEDRON（1974）引用：24

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7ChemInform Abstract: PROPELLANES PART 23, THE SYNTHESIS OF (4,4,3)PROPELLANES CONTAINING ONE CYCLOHEXADIENE RING

C. AMITH,J. KALO, B. E. NORTH,D. GINSBURG

AbstractDas Propelladien (II) wird aus dem bekannten Propellen (I) durch Bromierung mit N‐Bromsuccinimid (NBS) und anschließende Dehydrobromierung erhalten.

1974

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8Propellanes .23. Synthesis of [4.4.3]propellanes Containing One Cyclohexadiene Ring

C AMITH,J KALO, BE NORTH,D GINSBURG

Several propellanes containing in common a cyclohexane and a cyclohexadiene ring but varying in the structure of the third, 5-membered ring—an ether, a thioether, an anhydride or a methylimide ring—have been prepared.

1974TETRAHEDRON引用：7

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9Propellanes—XX

C. Amith,D. Ginsburg

1973Tetrahedron引用：3

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10Propellanes .20. Thermal Behavior Of 11,13-Dioxo-12-Methyl-12-Aza[4.4.3]Propella-2,4,7,9-Tetraenea

C Amith,D Ginsburg

1973TETRAHEDRON（1973）引用：6

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11Propellanes—XX: The thermal behavior of 11,3-dioxo-12-methyl-12-aza[4.4.3]Propella-2,4,7,9-tetraene

C. Amith,D. Ginsburg

The products formed by heating the title compound were isolated and their mode of formation is discussed.

1973Tetrahedron（1973）

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12ChemInform Abstract: PROPELLANES PART 20, THE THERMAL BEHAVIOR OF 11,13‐DIOXO‐12‐METHYL‐12‐AZA(4,4,3)PROPELLA‐2,4,7,9‐TETRAENE

C. AMITH,D. GINSBURG

AbstractBeim Erhitzen des Dioxoazapropellatetraens (I) in Dibutyläther‐Aceton im Bombenrohr entstehen neben dem bekannten Dimeren die Produkte (II) und (III) sowie (IV) (‐2% Ausbeute), (V) (2%), (VI) (2%) und (VII) (1%).

1973Chemischer Informationsdienst

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13An Application of Homonuclear Indor Spectroscopy

O SCIACOVELLI, PHILIPSB.WV,C AMITH,D GINSBURG

INDOR spectroscopy, a nuclear magnetic double resonance technique, is based upon the generalized nuclear Overhauser effect. It is shown that applied to protons this method is particularly useful for a precise determination of the frequencies of hidden lines and hence to obtain chemical shifts and coupling constants of these protons. In this way the structure of the dimer of 1a has been shown to be 3.

1970TETRAHEDRON（1970）引用：44

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