✦ LIBER ✦

Oxidative addition of trifluoromethanesulfonamide to cycloocta-1,3-diene. Ring contraction rearrangement

✍ Scribed by Moskalik, M. Yu.; Astakhova, V. V.; Ushakov, I. A.; Shainyan, B. A.

Book ID: 125395713
Publisher: SP MAIK Nauka/Interperiodica
Year: 2014
Tongue: English
Weight: 163 KB
Volume: 50
Category: Article
ISSN: 1070-4280
DOI: 10.1134/S1070428014030269

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Oxidative Addition of Tetrachloro-1,2-be

Oxidative Addition of Tetrachloro-1,2-benzoquinone to λ 3 -Cyclotriphosphazanes. An Unusual Ring Contraction−Rearrangement

✍ Thirupathi, Natesan; Krishnamurthy, Setharampattu S.; Nethaji, Munirathinam 📂 Article 📅 1999 🏛 American Chemical Society 🌐 English ⚖ 139 KB

Stereospecific double rearrangement of t

Stereospecific double rearrangement of trans-3,4-dimethyl-cis,trans-cycloocta-1,5-diene to cis-3,4-dimethyl-cis,cis-cycloocta-1,5-diene

✍ Berson, Jerome A.; Dervan, Peter B.; Jenkins, Jerry A. 📂 Article 📅 1972 🏛 American Chemical Society 🌐 English ⚖ 229 KB

Unexpected spontaneous ring-contraction

Unexpected spontaneous ring-contraction rearrangement of trifluoromethylated 1,2-oxazine N-oxides to 1-pyrroline N-oxides

✍ Vladislav Yu. Korotaev; Alexey Yu. Barkov; Pavel A. Slepukhin; Mikhail I. Kodess 📂 Article 📅 2011 🏛 Royal Society of Chemistry 🌐 English ⚖ 341 KB

Intramolecular carbenoid addition to 1,3

Intramolecular carbenoid addition to 1,3-dienes. Synthesis of cyclopentene annulated ring systems.

✍ T. Hudlicky; J.P. Sheth; V. Gee; D. Barnvos 📂 Article 📅 1979 🏛 Elsevier Science 🌐 French ⚖ 342 KB

Diazoketones containing a 1,3-diene moiety were decomposed to yield corresponding vinylcyclopropanes stereospecifically. Transformation of vinylcyclopropanes to cyclopentenes is described and the scope of the reaction is discussed. The intramolecular addition of carbenoids to conjugated dienes has n

ChemInform Abstract: Unexpected Spontane

ChemInform Abstract: Unexpected Spontaneous Ring-Contraction Rearrangement of Trifluoromethylated 1,2-Oxazine N-Oxides to 1-Pyrroline N-Oxides.

✍ Vladislav Yu. Korotaev; Alexey Yu. Barkov; Pavel A. Slepukhin; Mikhail I. Kodess 📂 Article 📅 2012 🏛 John Wiley and Sons ⚖ 29 KB 👁 2 views

## Abstract Reactions of cyclohexanone‐derived enamines (I) with nitrobutene (II) affords cyclic nitronates (III) instead of the expected isomeric nitrones of type (V).

Rearrangements in 1,3-dipolar additions

Rearrangements in 1,3-dipolar additions to 3,3-dimethylcycloproprene. The effect of ring strain on the rate of 1,3-dipoLar addition.

✍ Donald H. Aue; Gregory S. Helwig 📂 Article 📅 1974 🏛 Elsevier Science 🌐 French ⚖ 244 KB

We have found that 1,3-dipolar additions to 3,3-dimethylcyclopropene sometimes give rearranged products, but the rearrangement products all derive from a normal 1,3-dipolar adduct. Wo products from 3,3-dimethylcyclopropene or methylenecyclopropane' additions have been found that would correspond to