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Volumn 61, Issue 40, 2005, Pages 9569-9585

Intramolecular charge-transfer-induced chemiluminescent decomposition of 1,2-dioxetanes bearing a phenylmethanide anion

Author keywords

Carbanion; Chemiluminescence; Cyclopropanation; Dioxetane; Michael addition

Indexed keywords

1,2 DIOXETANE; 5 TERT BUTY 1 [3 (1 CYANOETHENYL)PHENYL] 4,4 DIMETHYL 2,6,7 TRIOXABICYCLO[3.2.0]HEPTANE; 5 TERT BUTYL 1 ARYL 4,4 DIMETHYL 2,6,7 TRIOXABICYCLO[3.2.0]HEPTANE; ANION; BIS(METHOXYCARBONYL)CHLOROMETHANIDE; BIS(METHOXYCARBONYL)METHANIDE; CARBENE; HEPTANE DERIVATIVE; METHANTHELINE BROMIDE; OXETANE DERIVATIVE; PHENYLMETHANIDE; TETRABUTYLAMMONIUM; UNCLASSIFIED DRUG;

EID: 27744470131     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2005.07.081     Document Type: Article
Times cited : (9)

References (28)
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    • Dihydrofurans (5) were synthesized easily from the corresponding 7-bromophenyl-2,2,4,4-tetramethyl-6-oxaheptan-3-one according to a procedure reported for related dihydrofurans [4b].
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    • Quinine bisulfate was used as the fluorescence standard.
  • 25
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    • Longman Scientific Technical: UK
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    • note
    • Rate constant reported in Ref. 9b is revised.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.