✦ LIBER ✦

Mass spectrometric analysis of N-substituted cyclohexene-1,2-dicarboximides

✍ Scribed by Earl D. Mitchell; George R. Waller

Publisher: John Wiley and Sons
Year: 1970
Tongue: English
Weight: 528 KB
Volume: 3
Category: Article
ISSN: 1076-5174
DOI: 10.1002/oms.1210030502

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The fusion of captan [N-(trichloromethyl

The fusion of captan [N-(trichloromethylthio)-4-cyclohexene-1,2-dicarboximide] with resorcinol

✍ I. Pomerantz; L. Miller; E. Lustig; D. Mastbrook; E. Hansen; R. Barron; N. Oates 📂 Article 📅 1969 🏛 Elsevier Science 🌐 French ⚖ 156 KB

Bromination of N-(o-Aminophenyl)-cis-4-c

Bromination of N-(o-Aminophenyl)-cis-4-cyclohexene-1,2-dicarboximide and cis-2-(2-Benzimidazolyl)-4-cyclohexene-1-carboxylic Acid.

✍ S. I. Idrisova 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 86 KB 👁 2 views

ChemInform Abstract: Diels—Alder Reactio

ChemInform Abstract: Diels—Alder Reactions of Hexachlorocyclopentadiene with N-Hydroxy- and N-Hydroxyalkyl-cis-4-cyclohexene-1,2-dicarboximides.

✍ M. S. Salakhov; R. G. Agadzhanov; V. S. Umaeva 📂 Article 📅 2000 🏛 John Wiley and Sons ⚖ 31 KB 👁 1 views

Mass-spectrometric behavior of N-substit

Mass-spectrometric behavior of N-substituted 2-methyl-3-acetyl pyrroles

✍ E. A. Runova; N. M. Tanchuk; P. B. Terent'ev; A. A. Bratkov; M. M. Vartanyan; é. 📂 Article 📅 1987 🏛 Springer US 🌐 English ⚖ 208 KB

Synthesis, properties, and mass-spectrom

Synthesis, properties, and mass-spectrometric behavior of 6-substituted imidazo[1,2-f]xanthines

✍ S. N. Garmash; B. A. Priimenko; E. A. Skul'skaya; N. A. Klyuev; N. V. Koval' 📂 Article 📅 1987 🏛 Springer US 🌐 English ⚖ 389 KB

Mass spectrometric determination of the

Mass spectrometric determination of the configuration of the 4-substituted 1,2-dimethyl-4-hydroxydecahydroquinolines

✍ V. G. Zaikin; N. S. Wulfson; V. I. Zaretskii; A. A. Bakaev; A. A. Akhrem; L. I. 📂 Article 📅 1969 🏛 John Wiley and Sons 🌐 English ⚖ 320 KB

The mass spectra of a number of the epimeric 1,2-dimethyl-4-alkyl-4-hydroxydecahydroquinolines (alkyl: C z C H , CH=CH,, C,H, and COCH,) have been studied. The configuration at C-2 and C-4 in these molecules is proposed on the basis of the data obtained. Some aspects of the fragmentation pathways un