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Volumn 46, Issue 3, 2007, Pages 467-469

Organocatalytic one-pot asymmetric synthesis of functionalized tricyclic carbon frameworks from a triple-cascade/Diels-Alder sequence

Author keywords

Asymmetric synthesis; Cycloaddition; Domino reactions; Multicomponent reactions; Organocatalysis

Indexed keywords

ADDITION REACTIONS; CARBON; CATALYSIS; CHEMICAL BONDS; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

EID: 33846429586     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200603434     Document Type: Article
Times cited : (252)

References (51)
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    • 819, and references therein;
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    • For reviews on the Diels-Alder reaction, see: a) E. J. Corey, Angew. Chem. 2002, 114, 1724;
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    • 33846458110 scopus 로고    scopus 로고
    • for IMDA reviews, see: c W. R. Roush in Comprehensive Organic Synthesis, 5 (Eds.: B. M. Trost, I. Fleming), Pergamon, Oxford, 1991, pp. 513-550;
    • for IMDA reviews, see: c) W. R. Roush in Comprehensive Organic Synthesis, Vol. 5 (Eds.: B. M. Trost, I. Fleming), Pergamon, Oxford, 1991, pp. 513-550;
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    • For organocatalyzed IMDA reactions of triene aldehydes, see: a
    • For organocatalyzed IMDA reactions of triene aldehydes, see: a) R. M. Wilson, W. S. Jen, D. W. C. MacMillan, J. Am. Chem. Soc. 2005, 127, 11 616;
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    • For studies on the outcome of IMDA reactions, see: a
    • For studies on the outcome of IMDA reactions, see: a) Ref. [13c];
    • , vol.13 c
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    • All novel compounds were fully characterized m.p, optical rotation, NMR, IR, MS, and elemental analyses, and the spectroscopic and analytical data are in agreement with the assigned structures
    • All novel compounds were fully characterized (m.p., optical rotation, NMR, IR, MS, and elemental analyses), and the spectroscopic and analytical data are in agreement with the assigned structures.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.