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Volumn 130, Issue 30, 2008, Pages 10024-10029

Bioinspired polyene cyclization promoted by intermolecular chiral acetal-SnCl4 or chiral N-acetal-TiCl4: Investigation of the mechanism and identification of the key intermediates

Author keywords

[No Author keywords available]

Indexed keywords

BIO-INSPIRED; LEWIS ACIDS;

EID: 48249135712     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja802896n     Document Type: Article
Times cited : (40)

References (87)
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    • For an English translation and historical perspective on the 50th Anniversary of the Eschenmoser, Ruzika, Jeger, and Arigoni 1955 paper, see: (c) Eschenmoser, A.; Arigoni, D. Helv. Chim. Acta 2005, 88, 3011-3050.
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    • For reviews about N-acyliminium fromN-acetal initiated cyclization, see: (a) Maryanoff, B. E.; Zhang, H. C.; Cohen, J. H.; Turchi, I. J.; Maryanoff, C. A. Chem. Rev. 2004, 104, 1431-1628.
    • For reviews about N-acyliminium fromN-acetal initiated cyclization, see: (a) Maryanoff, B. E.; Zhang, H. C.; Cohen, J. H.; Turchi, I. J.; Maryanoff, C. A. Chem. Rev. 2004, 104, 1431-1628.
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    • The chiral N-acetal was synthesized from optical pure 1,2-hydroxy amine using the modified Didier's procedure: (a) Didier, E.; Fouque, E.; Taillepied, I.; Commercon, A. Tetrahedron Lett. 1994, 35, 2349-2352.
    • The chiral N-acetal was synthesized from optical pure 1,2-hydroxy amine using the modified Didier's procedure: (a) Didier, E.; Fouque, E.; Taillepied, I.; Commercon, A. Tetrahedron Lett. 1994, 35, 2349-2352.
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    • For structure detail of ketone 13, see Supporting Information.
    • For structure detail of ketone 13, see Supporting Information.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.