ChemInform Abstract: HETEROCYCLIC SEVEN-MEMBERED RING COMPOUNDS. XV. THERMAL REARRANGEMENT OF A 2-METHYL-1-BENZOXEPIN, A CONTRIBUTION TO THE SEARCH FOR INTERMEDIATES IN THE 1-BENZOXEPIN-NAPHTHOL REARRANGEMENT

1976 ◽  
Vol 7 (6) ◽  
pp. no-no
Author(s):  
HANS HOFMANN ◽  
PETER HOFMANN
1990 ◽  
Vol 45 (7) ◽  
pp. 1059-1066 ◽  
Author(s):  
Hans Hofmann ◽  
Christine Göttfert ◽  
Helmut Gaube

Thermodynamic Data, Heterocyclic Seven-Membered Ring CompoundsOn heating in carbon tetrachloride or nitromethane the 5-methoxy-1-benzothiepines 1-4 isomerize to the corresponding thionaphtholes 5-8, whereas in cyclohexane from 1-4 the usual desulfuration products C arise. Kinetic and thermodynamic data have been estimated for the reactions 3 → 7 and 4 → 8. If the thermal rearrangement of 3 resp. 4 takes place in presence of cyclohexene sulphide, one gets the desulfuration products C also in carbon tetrachloride or nitromethane as solvent together with the equimolar amount of cyclohexene. This behaviour leads to the assumption of a S2-spezies as the primary elimination product of sulphur from the episulphide intermediate A.


1990 ◽  
Vol 45 (11) ◽  
pp. 1573-1576 ◽  
Author(s):  
Hans Hofmann ◽  
Herbert Fischer ◽  
Markus de Vries

Reaction of 1-benzothiepine (4), whose synthesis has been improved, with trimethyloxonium tetrafluoroborate yields 1-methyl-1-benzothiepinium tetrafluoroborate (5). Compound 5 rearranges to methyl 1-naphthyl sulfide (6) on heating in acetonitrile. The reaction rate 5 → 6 was determined at one temperature (75°C).


2019 ◽  
Author(s):  
Gabriel da Silva

Atmospheric oxidation of isoprene produces significant yields of eight unique nitrate 11 compounds, each with a β- or δ-hydroxy group. These isoprene hydroxy nitrates (ISOPNs) 12 significantly impact upon global NOx budgets, O3 levels, and aerosol formation. 13 Uncertainties exist, however, in our understanding of ISOPN chemistry, particularly in their 14 yields from the reaction of isoprene peroxyl radicals with NO. This study describes novel 15 isomerization reactions of the ISOPNs, identified through the application of computational 16 chemistry techniques. These reactions produce saturated polycyclic orthonitrite compounds 17 via attack of the R–NO2 group on the vinyl moiety. For the δ-hydroxy nitrates, low-energy 18 isomerization pathways exist to six-membered ring compounds that are around 5 kcal mol-1 19 exothermic. These reactions proceed with barriers around 15 kcal mol-1 below the 20 respective peroxyl radical + NO reactants and yield orthonitrites that can further isomerize 21 to β-hydroxy ISOPNs. Moreover, the δ-hydroxy nitrates can directly interconvert with their β 22 substituted counterparts via NO3 group migration, with barriers that are lower yet. It follows 23 that β-hydroxy nitrates may be stabilized in the δ-hydroxy form, and vice versa. Moreover, 24 the lowest-energy pathway for dissociation of the δ-hydroxy ISOPNs is for the formation of 25 β-hydroxy alkoxyl radicals, and because of this established branching fractions between the 26 various isoprene peroxyl radicals may require re-evaluation. The results presented here also 27 suggest that ISOPNs may be stabilized to some extent in their saturated orthonitrite forms, 28 which has implications for both the total nitrate yield and for their subsequent removal by 29 OH, O3, and photolysis.<br><br>


2021 ◽  
Vol 57 (29) ◽  
pp. 3603-3606
Author(s):  
Florent Bodinier ◽  
Youssouf Sanogo ◽  
Janick Ardisson ◽  
Marie-Isabelle Lannou ◽  
Geoffroy Sorin

Herein, we describe unprecedented access to all-carbon or heterocyclic seven-membered ring frameworks from 1,8-ene-ynes promoted by inexpensive low-valent titanium(ii) species, readily available from a combination of Ti(OiPr)4 and Grignard reagent.


Synlett ◽  
2021 ◽  
Author(s):  
Memg Wang ◽  
Changxu Zhong ◽  
Ping Lu

Enantioselective synthesis of cyclobutane derivatives is still a challenging topic in asymmetric synthesis. [2+2]-Cycloaddition and skeleton rearrangement are two primary strategies to this end. Recently, functionalization of cyclobutanones and cyclobutenones, which are readily available via [2+2]-cycloadditions as prochiral substrates, has emerged as a powerful tool to access versatile four-membered ring compounds. Herein, we summarize some recent advances in these areas from our and other groups.


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