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Volumn 43, Issue 18, 2004, Pages 2420-2423

Synthesis of β-hydroxyaldehydes with stereogenic quaternary carbon centers by direct organocatalytic asymmetric aldol reactions

Author keywords

Aldol reaction; Asymmetric catalysis; Enantioselectivity; High throughput screening; Organocatalysis

Indexed keywords

ALDEHYDES; BROMINE; CATALYSTS; CHLORINE; FLUORESCENCE; NITROGEN OXIDES;

EID: 3042625080     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200353546     Document Type: Article
Times cited : (247)

References (43)
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    • For selected studies of the Michael reaction, see: a) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685-689; Angew. Chem. Int. Ed. 2003, 42, 661-665;
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    • For selected studies of the Michael reaction, see: a) N. Halland, P. S. Aburel, K. A. Jørgensen, Angew. Chem. 2003, 115, 685-689; Angew. Chem. Int. Ed. 2003, 42, 661-665;
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 661-665
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    • For studies of the Diels-Alder reaction, see: a) D. B. Ramachary, N. S. Chowdari, C. F. Barbas III, Angew. Chem. 2003, 115, 4365-4369; Angew. Chem. Int. Ed. 2003, 42, 4233-4237;
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    • b) K. Juhl, K. A. Jørgensen, Angew. Chem. 2003, 115, 1536-1539; Angew. Chem. Int. Ed. 2003, 42, 1498-1501;
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    • note
    • For the introduction of a chiral tertiary hydroxy group at the β position to the carbonyl group by using organocatalysis, see reference [3h]; see also references [3d], [5b], and [5c].
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    • note
    • 2H for further study.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.