✦ LIBER ✦

ChemInform Abstract: Reaction of Dichlorocarbene with 2,3-Dihydro-5,6-dimethyl-1,4-oxathiin and 2,3-Dihydro-5,6-dimethyl-1,4-dithiin.

✍ Scribed by A. D. BREWER; A. A. ZNOTINS

Book ID: 112034906
Publisher: John Wiley and Sons
Year: 2010
Weight: 28 KB
Volume: 27
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.199630055

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Reaction of dichlorocarbene with 2,3-dih

Reaction of dichlorocarbene with 2,3-dihydro-5,6-dimethyl-1,4-oxathiin and 2,3-dihydro-5,6-dimethyl-1,4-dithiin

✍ A. D. Brewer; A. A. Znotins 📂 Article 📅 1996 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 157 KB

2,3-Dihydro-5,6-dimethyl-1,4-dithiin 1,1

2,3-Dihydro-5,6-dimethyl-1,4-dithiin 1,1,4,4-tetroxide

✍ Arora, S. K. ;Bates, R. B. ;Kriek, G. ;Brewer, A. D. 📂 Article 📅 1978 🏛 International Union of Crystallography ⚖ 277 KB

2,3-Dihydro-5,6-dimethyl-1,4-dithiine

2,3-Dihydro-5,6-dimethyl-1,4-dithiine 1,1,4-trioxide

✍ Strunk, Richard J. ;Brewer, A. David ;Ferguson, George ;Lough, Alan J. 📂 Article 📅 2004 🏛 International Union of Crystallography 🌐 English ⚖ 146 KB

5,6-Dihydro-1,3-dimethyl-5,6-bis[1',3'-d

5,6-Dihydro-1,3-dimethyl-5,6-bis[1',3'-dimethyl-2',4',6'-trioxopyrimid(5,5')yl]furo[2,3-d]uracil

✍ Poling, M. ;Van der Helm, D. 📂 Article 📅 1976 🏛 International Union of Crystallography ⚖ 259 KB

Diethyl 2,6-dimethyl-4-phenyl-1,4-dihydr

Diethyl 2,6-dimethyl-4-phenyl-1,4-dihydro-3,5-pyridinedicarboxylate

✍ Hempel, A. ;Gupta, M. P. 📂 Article 📅 1978 🏛 International Union of Crystallography ⚖ 293 KB

Electron impact induced fragmentation of

Electron impact induced fragmentation of dihydro-1,4-oxathiines. 1. 2,3-substituted 5,6-dihydro-1,4-oxathiines

✍ Vesa Nevalainen; Pirjo Vainiotalo 📂 Article 📅 1986 🏛 John Wiley and Sons 🌐 English ⚖ 709 KB

In the electron impact induced fragmentation of 2,3-disubstituted 5,6-dihydro-1,4-oxathiines, the cleavage of the heterocyclic ring proceeds through the retro Diels-Alder type of reaction. The further fragmentation of the resulting radical cation gives rise to substituted carbonyl or thiocarbonyl ca