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Volumn 13, Issue 8, 2011, Pages 2012-2014

Iron(II) triflate as a catalyst for the synthesis of indoles by intramolecular C-H amination

Author keywords

[No Author keywords available]

Indexed keywords

CARBON; HYDROGEN; INDOLE; INDOLE DERIVATIVE; IRON; IRON(II) TRIFLATE; MESYLIC ACID DERIVATIVE;

EID: 79955377801     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol2004066     Document Type: Article
Times cited : (145)

References (57)
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    • Simoneau, C.A.1    Ganem, B.2
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    • For a review on nitrene chemistry, see: Söderberg, B. C. G. Curr. Org. Chem. 2000, 4, 727.
    • (2000) Curr. Org. Chem. , vol.4 , pp. 727
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    • For other iron-catalyzed reactions with nonaromatic azides.
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    • 2H-Azirines were shown to undergo ring opening to give indoles under iron catalysis. Also here, iron nitrenes have been suggested as intermediates
    • 2H-Azirines were shown to undergo ring opening to give indoles under iron catalysis. Also here, iron nitrenes have been suggested as intermediates. Jana, S.; Clements, M. D.; Sharp, B. K; Zheng, N. Org. Lett. 2010, 12, 3736
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  • 39
    • 79955413837 scopus 로고    scopus 로고
    • In this study, commercially available iron(II) triflate (98% from abcr) was used
    • In this study, commercially available iron(II) triflate (98% from abcr) was used.
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    • 20TPP stands for meso-tetrakis- (pentafluorophenyl)porphyrin] in toxic 1,2-dichloroethan was used as a catalyst
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.