7-Azatetracyclo[4.1.0.02,4.03,5]heptan

Christl, Manfred; Leininger, Hartmut

doi:10.1016/s0040-4039(01)93588-9

Cited by 12 publications

(4 citation statements)

References 15 publications

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“…Rearrangements leading to azepines from five-mem- cycloadducts110,obtainedfromDMADandpyrroles,arephotochemicallyconvertedinto thermally unstable azaquadricyclanes, which rearrange to the substituted 1H-azepine derivatives 111 [134]. The other two examples concern the synthesis of the 1-phenyl-1H-azepine 113 by thermal decomposition of the triazole derivative 112 [135] and the preparation of azepinones 115 by ring expansion of the dioxopyrrole derivatives 114 [136].…”

Section: Grubbs I Grubbs Iimentioning

confidence: 99%

Seven‐Membered Heterocycles: Azepines, Benzo Derivatives and Related Systems

Vaquero

Cuadro

Herradón

2011

Modern Heterocyclic Chemistry

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The replacement of a carbon atom by a heteroatom in a seven-membered carbocycle leads to the corresponding seven-membered heterocyclic ring system. Different types of heterocycles can be formed depending on the nature of the carbocycle. In a cycloheptatriene the replacement can involve any of the six sp 2 hybridized carbons or the sp 3 carbon atom, whereas in cycloheptane all carbon atoms are equivalent and replacement affords exclusively the fully saturated heterocyclic systems. Partially saturated seven-membered heterocycles can be viewed as derivatives or related systems of these two main seven-membered heterocyclic units arising from carbon replacement in cycloheptatriene and in cycloheptane. Replacement of the sp 3 hybridized carbon atom in cycloheptatriene by a nitrogen leads to an azacycloheptatriene known as 1H-azepine (1) and the corresponding 2H-, 3H-, and 4H-azepines (2-4) are the tautomeric forms generated by the replacement of the sp 2 carbons. 1H-Azepine is an unstable red oil that is prone to rearrange to the also unstable 3H-azepine in the presence of acids and bases. However, this tautomer seems to be more stable than both 4H-and 2H-azepine. The structures related to 1H-azepine that bear an oxygen or sulfur atom are known as oxepine (5) and thiepine (6) (thiepin is favored by Chemical Abstracts Service). Oxepine is much more stable than thiepine and has been synthesized, isolated, and characterized at room temperature while thiepine has not been detected to date. Stable monocyclic thiepines were prepared and characterized in the 1980s. Azepines, oxepines, and thiepines that are constrained to planar or almost planar conformations should be antiaromatic molecules with negative resonance energy and, as a consequence, these compounds are unknown.The fully saturated seven-membered heterocycle containing one nitrogen is azepane (7) (hexahydroazepine or perhydroazepine); the oxygen and sulfur analogues are known as oxepane (8) and thiepane (9). All of these compounds are stable and show typical behavior of secondary amine, ether and thioether, respectively. TwoModern Heterocyclic Chemistry, First Edition. Edited

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Section: Grubbs I Grubbs Iimentioning

confidence: 99%

Seven‐Membered Heterocycles: Azepines, Benzo Derivatives and Related Systems

Vaquero

Cuadro

Herradón

2011

Modern Heterocyclic Chemistry

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“…13') 2-Aza-barrelene an. Nach STO-3G-Rechnungen haben 2-Aza-barrelen (3) (2) (Ausb. 6-8%, farbloses Kristallpulver, F p = 151 "C (Sublimation bei 80 "C/O.Ol mbar)) (siehe Tabelle 1).…”

Section: Von Rudolf Gompper Und Axel Schmidt['] Professor Rolf Huisgeunclassified

“…Die Umwandlung von (2) in 3-Methoxy-2-aza-bicyclo [2.2.2]octa-2,5,7-trien (3-Methoxy-2-aza-barrelen) (9) (Ausb. 75%, farbloses, angenehm eukalyptusartig/,,aromatisch" riechendes 01, K p = 80 oC/O.Ol mbar) (siehe Tabelle 1) gelingt schliefilich mit Trimethyloxonium-tetrafluoroborat nach bekanntem Verfahren (vgl.…”

Section: Von Rudolf Gompper Und Axel Schmidt['] Professor Rolf Huisgeunclassified

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