✦ LIBER ✦

The 1H NMR spectrum of [1-13C]butadiene-1,3

✍ Scribed by G Schrumpf; G Becher; W Lüttke

Publisher: Elsevier Science
Year: 1973
Weight: 276 KB
Volume: 10
Category: Article
ISSN: 0022-2364
DOI: 10.1016/0022-2364(73)90239-4

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

13C13C-Kopplungskonstanten von 1,3-Butad

13C13C-Kopplungskonstanten von 1,3-Butadien

✍ Georg Becher; Wolfgang Lüttke; Dr. Gerd Schrumpf 📂 Article 📅 1973 🏛 John Wiley and Sons 🌐 English ⚖ 235 KB 👁 1 views

13C13C Coupling Constants of 1,3-Butadie

13C13C Coupling Constants of 1,3-Butadiene

✍ Dipl.-Chem. Georg Becher; Prof. Dr. Wolfgang Lüttke; Dr. Gerd Schrumpf 📂 Article 📅 1973 🏛 John Wiley and Sons 🌐 English ⚖ 232 KB 👁 1 views

Assignment of the 13C NMR spectrum of an

Assignment of the 13C NMR spectrum of anisomycin and the 1H and 13C NMR spectra of deacetylanisomycin

✍ J. W. LeFevre; S. E. Maier; W. Deng 📂 Article 📅 1993 🏛 John Wiley and Sons 🌐 English ⚖ 260 KB

## Abstract The ^13^C NMR spectrum of anisomycin and the ^1^H and ^13^C NMR spectra of deacetylanisomycin were assigned using one‐ and two‐dimensional NMR analysis. The techniques included INEPT, ^1^H^13^C HETCORR and ^1^H‐^1^H COSY spectroscopy.

Winnowing the {13C}-1H resonances in the

Winnowing the {13C}-1H resonances in the in Vivo NMR spectrum

✍ T Jue 📂 Article 📅 1987 🏛 Elsevier Science ⚖ 369 KB

1H and 13C NMR studies on 1,3,2-dioxarso

1H and 13C NMR studies on 1,3,2-dioxarsolanes

✍ D. W. Aksnes; A. Lie 📂 Article 📅 1983 🏛 John Wiley and Sons 🌐 English ⚖ 760 KB

The 'H and -C NMR spectra of a series of 1,3,2-dioxarsolanes have been obtained at 2.1T and some at 9.4T. The chemical shifts and spin-spii coupling constants have been obtained from complete spectral analyw of the 'H and proton-coupled -C spectra. The spectral data are interpreted on the basis of t

1H and 13C NMR spectroscopy of substitut

1H and 13C NMR spectroscopy of substituted 1,2,3-triazoles

✍ Xiao-Wen Sun; Peng-Fei Xu; Zi-Yi Zhang 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 153 KB 👁 1 views

1-Aryl-4-carboxy-5-methyl-1,2,3-triazoles were prepared by the condensation of aryl azides with ethyl acetoacetate. The structures of these compounds were characterized by MS, IR and 1H and 13C NMR spectroscopy. The measured and calculated 13C chemical shifts of the aromatic carbons were compared.