σ-bishomoaromatic heterocycles: Reactivity and synthesis of 3-oxatetracyclo[3.3.0.02,804,6]octane by photolysis at 185 nm

Tetrahedron Letters

Volumn 37, Issue 9, 1996, Pages 1385-1388

  Klärner, Frank Gerrit ^a   Dolz, Thomas ^a   Uhländer, Christoph ^a   Yaslak, Salih ^b  

^a UNIVERSITY OF DUISBURG ESSEN   (Germany)

^b MARMARA UNIVERSITY   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

NORBORNENE DERIVATIVE;

ARTICLE; DRUG SYNTHESIS; NUCLEAR MAGNETIC RESONANCE; PHOTOCHEMISTRY; REACTION ANALYSIS;

EID: 0029965831     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(96)00062-7     Document Type: Article

References (28)

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11. +).
12. 2 to 2-oxabicyclo[3.2.0]hepta-3,6-diene followed by photolysis of the adduct) undergoes a thermal rearrangement to 4-oxabicyclo[5.1.0]octa-2,5-diene which is explained by a sequence of 1,4-electrocyclic ring-opening leading to 20 followed by a [1,6] carbon shift. . Weubel, G., Dissertation, Ruhr Universität Bochum, 1992 (research director: F.-G. Klärner).
13. 2 to 2-oxabicyclo[3.2.0]hepta-3,6-diene followed by photolysis of the adduct) undergoes a thermal rearrangement to 4-oxabicyclo[5.1.0]octa-2,5-diene which is explained by a sequence of 1,4-electrocyclic ring-opening leading to 20 followed by a [1,6] carbon shift. . Weubel, G., Dissertation, Ruhr Universität Bochum, 1992 (research director: F.-G. Klärner).
14. 2 to 2-oxabicyclo[3.2.0]hepta-3,6-diene followed by photolysis of the adduct) undergoes a thermal rearrangement to 4-oxabicyclo[5.1.0]octa-2,5-diene which is explained by a sequence of 1,4-electrocyclic ring-opening leading to 20 followed by a [1,6] carbon shift. . Weubel, G., Dissertation, Ruhr Universität Bochum, 1992 (research director: F.-G. Klärner).
15. 2 to 2-oxabicyclo[3.2.0]hepta-3,6-diene followed by photolysis of the adduct) undergoes a thermal rearrangement to 4-oxabicyclo[5.1.0]octa-2,5-diene which is explained by a sequence of 1,4-electrocyclic ring-opening leading to 20 followed by a [1,6] carbon shift. . Weubel, G., Dissertation, Ruhr Universität Bochum, 1992 (research director: F.-G. Klärner).
16. 2 to 2-oxabicyclo[3.2.0]hepta-3,6-diene followed by photolysis of the adduct) undergoes a thermal rearrangement to 4-oxabicyclo[5.1.0]octa-2,5-diene which is explained by a sequence of 1,4-electrocyclic ring-opening leading to 20 followed by a [1,6] carbon shift. . Weubel, G., Dissertation, Ruhr Universität Bochum, 1992 (research director: F.-G. Klärner).
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