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Volumn , Issue 5, 2004, Pages 765-774

Synthesis of enantiomerically and diastereomerically pure 4-hydroxy-1,2-alkadienyl carbamates and their application in a modified nazarov cyclization towards chiral cyclopentenones

Author keywords

Allenes; Carbamates; Cyclizations; Cyclopentenones; Diastereoselectivity; Nazarov reactions

Indexed keywords

MOLECULAR ORIENTATION; ORGANIC COMPOUNDS; POLYURETHANES; REACTION KINETICS; SUBSTITUTION REACTIONS; SYNTHESIS (CHEMICAL);

EID: 1942489143     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2004-816002     Document Type: Article
Times cited : (29)

References (37)
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    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 2933
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    • For reviews, see: (a) Patai, S. The Chemistry of Ketenes, Allenes, and Related Compounds; Wiley: Chichester, 1980. (b) Schuster, H. F.; Coppola, G. M. Allenes in Organic Synthesis; Wiley: New York, 1984. (c) Landor, S. R. The Chemistry of the Allenes; Academic Press: New York, 1982. (d) Hoffmann-Röder, A.; Krause, N. Angew. Chem. Int. Ed. 2002, 41, 2933; Angew. Chem. 2002, 114, 3057.
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    • Programs used for X-ray crystal structure analysis of 18: data collection EXPRESS (Nonius B.V., 1994), data reduction MolEN (K. Fair, Enraf-Nonius B.V., 1990), structure solution SHELXS-97 (Sheldrick, G. M. Acta Crystalogr. Sect. A 1990, 46, 467), structure refinement SHELXL-97 (G. M. Sheldrick, Universität Göttingen, 1997), graphics SCHAKAL (E. Keller, Universität Freiburg, 1997). Crystallographic data (excluding structure factors) for the structure reported in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication no. CCDC-229908. Copies of the data can be obtained free of charge on application to The Director, CCDC, 12 Union Road, CambridgeCB2 1EZ, UK [fax: int. code +44(1223)336-033; e-mail: deposit@ccdc.cam.ac.uk].
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    • note
    • Yields of compound (Z,R)-25 and (Z,R)-26 are based on enone 20a.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.