✦ LIBER ✦

Mass spectra of new functionally substituted heterocycles: VI. Fragmentation of 3-methoxy-7-methyl-2-methylsulfanyl-4,5-dihydro-3H-azepine, its structural isomers, 5-methoxy-2,2-dimethyl-6-methylsulfanyl-2,3-dihydropyridine and 1-isopropyl-3-methoxy-2-methylsulfanyl-1H-pyrrole, and their linear precursors under electron impact

✍ Scribed by L. V. Klyba; N. A. Nedolya; E. R. Zhanchipova

Book ID: 111464577
Publisher: SP MAIK Nauka/Interperiodica
Year: 2008
Tongue: English
Weight: 246 KB
Volume: 44
Category: Article
ISSN: 1070-4280
DOI: 10.1134/s1070428008010181

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Mass spectra of new heterocycles: IX. Ma

Mass spectra of new heterocycles: IX. Main fragmentaion laws of 7-methyl-2-(methylsulfanyl)-3-(1-ethoxyethoxy)-4,5-dihydro-3H-azepine and its structural isomers (2,3-dihydropyridine, pyrrole, thiophene) under electron impact

✍ L. V. Klyba; N. A. Nedolya; O. A. Tarasova; E. R. Zhanchipova; O. G. Volostnykh 📂 Article 📅 2010 🏛 SP MAIK Nauka/Interperiodica 🌐 English ⚖ 572 KB

Reactions of lithiated allenes with isot

Reactions of lithiated allenes with isothiocyanates: First example of deprotonation of 2-aza-1,3,5-trienes. Synthesis of 6-methoxy-2-methyl-3H-azepine and 3-methoxy-7-methyl-2-methylsulfanyl-4,5-dihydro-3H-azepine

✍ N. A. Nedolya; L. L. Dmitrieva; A. I. Albanov; L. V. Klyba; O. A. Tarasova; I. A 📂 Article 📅 2006 🏛 SP MAIK Nauka/Interperiodica 🌐 English ⚖ 130 KB

Reactions of Lithiated Allenes with Isot

Reactions of Lithiated Allenes with Isothiocyanates: First Example of Deprotonation of 2-Aza-1,3,5-trienes. Synthesis of 6-Methoxy-2-methyl-3H-azepine and 3-Methoxy-7-methyl-2-methylsulfanyl-4,5-dihydro-3H-azepine.

✍ N. A. Nedolya; L. L. Dmitrieva; A. I. Albanov; L. V. Klyba; O. A. Tarasova; I. A 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 15 KB 👁 2 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.