✦ LIBER ✦

Difference in the Behavior of 1'-Methyl-1',4'-dihydro-2,3'-diquinolyl in Its Reactions with Sulfur and Selenium

✍ Scribed by D. V. Moiseev; A. V. Aksenov

Book ID: 110335709
Publisher: Springer US
Year: 2002
Tongue: English
Weight: 89 KB
Volume: 38
Category: Article
ISSN: 0009-3122
DOI: 10.1023/a:1015316015108

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Difference in the Behavior of 1′-Methyl-

Difference in the Behavior of 1′-Methyl-1′,4′-dihydro-2,3′-diquinolyl in Its Reactions with Sulfur and Selenium.

✍ D. V. Moiseev; A. V. Aksenov 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 26 KB 👁 1 views

Formation of 2,3-dihydro-3-chloromethyln

Formation of 2,3-dihydro-3-chloromethylnaphtho[1,2-b][1,4]-dithiane in the reaction of allyl 1-naphthyl sulfide with sulfur dichloride

✍ N. V. Fedorov; A. A. Grishkin; A. V. Anisimov; E. A. Viktorova 📂 Article 📅 1990 🏛 Springer US 🌐 English ⚖ 59 KB

Kinetic resolution of (±)-2,3-dihydro-3-

Kinetic resolution of (±)-2,3-dihydro-3-methyl-4H-1,4-benzoxazine in the reaction with (S)-naproxen chloride: a theoretical study

✍ Vladimir A. Potemkin; Victor P. Krasnov; Galina L. Levit; Ekaterina V. Bartashev 📂 Article 📅 2004 🏛 Royal Society of Chemistry 🌐 English ⚖ 104 KB

Reactions of selenium dichloride and dib

Reactions of selenium dichloride and dibromide with unsaturated ethers. Annulation of 2,3-dihydro-1,4-oxaselenine to the benzene ring

✍ Vladimir A. Potapov; Maxim V. Musalov; Svetlana V. Amosova 📂 Article 📅 2011 🏛 Elsevier Science 🌐 French ⚖ 439 KB

Formation of 3,4,5,6-tetrahydroquinazoli

Formation of 3,4,5,6-tetrahydroquinazolin-2(1H)-one derivatives in reaction of 4-aryl-6-methyl-3,4-dihydro-pyrimidin-2(1H)-ones with chalcones

✍ Kolosov, M. A.; Kulyk, O. G.; Starchenko, O. I.; Orlov, V. D. 📂 Article 📅 2013 🏛 Springer US 🌐 English ⚖ 318 KB

1,2-Methyl shift in the reaction of 4,7-

1,2-Methyl shift in the reaction of 4,7-dihydro-4,5-dimethyl-7-phenyl-(1,2,4)-triazolo[1,5-a]pyrimidine with tosyl azide

✍ Sergey A. Komykhov; Sergey M. Desenko; Alexander S. Kaganovsky; Valery D. Orlov; 📂 Article 📅 2000 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 115 KB

## Abstract The reaction of the heterocyclic enamine **1** with tosyl azide (**2**) leads to the tosylimino derivative **4** of 1,2,4‐triazolo[1,5‐a]pyrimidine. The extrusion of nitrogen from the primary adduct **3** is followed by a 1,2‐shift of a methyl group. The structure determination of **4**