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Volumn , Issue 18, 2007, Pages 2964-2969

Structure determination of photoproducts of anthracenes with (Arylmethoxymethyl) sidechains

Author keywords

Cyclization; Cyclodimerization; Photochemistry; Regioselectivity; Rotamers

Indexed keywords


EID: 34347361756     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.200700140     Document Type: Article
Times cited : (9)

References (38)
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    • 1H-NMR spectrum of the raw reaction product 5b contains a trace of 4b.
    • 1H-NMR spectrum of the raw reaction product 5b contains a trace of 4b.
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    • Allusively the splitting of this signal can be seen in a resolution-enhanced output of the FID free induction decay
    • Allusively the splitting of this signal can be seen in a resolution-enhanced output of the FID (free induction decay).
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    • The coalescence temperatures of the signals permit a rough estimation of the activation barrier of the restricted rotation: ΔG ≠, 66 ± 5 kJ mol-1
    • -1.
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    • The reverse photochemical reaction 5→ 3 is not sufficiently straightforward for an optical switch.
    • The reverse photochemical reaction 5→ 3 is not sufficiently straightforward for an optical switch.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.