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Volumn 128, Issue 1, 2006, Pages 48-49

Tris(trimethylsilyl)silyl-governed aldehyde cross-aldol cascade reaction

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; POLYKETIDE;

EID: 30744464122     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja054725k     Document Type: Article
Times cited : (167)

References (28)
  • 2
    • 0007423794 scopus 로고
    • Adams, R., Blatt, A. H., Boekelheide, V., Cairns, T. L., Cram, D. J., House H. O., Eds.; John Wiley & Sons: New York
    • For reviews of aldol reaction, see: (a) Nielsen, A. T.; Houlihan, W. J. In Organic Reaction: Adams, R., Blatt, A. H., Boekelheide, V., Cairns, T. L., Cram, D. J., House H. O., Eds.; John Wiley & Sons: New York, 1968; Vol. 16.
    • (1968) Organic Reaction , vol.16
    • Nielsen, A.T.1    Houlihan, W.J.2
  • 3
    • 0000145196 scopus 로고
    • Dauben, W. G., et al., Eds.; John Wiley & Sons; New York
    • (b) Mukaiyama, T. In Organic Reactions; Dauben, W. G., et al., Eds.; John Wiley & Sons; New York, 1982; Vol. 28, pp 203-331
    • (1982) Organic Reactions , vol.28 , pp. 203-331
    • Mukaiyama, T.1
  • 4
    • 0000851696 scopus 로고
    • Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford
    • (c) Heathcock, C. H. In Comprehensive Organic Synthesis, Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford, 1991; Vol 2, pp 133-238
    • (1991) Comprehensive Organic Synthesis , vol.2 , pp. 133-238
    • Heathcock, C.H.1
  • 5
    • 0001316868 scopus 로고
    • Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford
    • (d) Gennari, C. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford, 1991; Vol 2, pp 629-660.
    • (1991) Comprehensive Organic Synthesis , vol.2 , pp. 629-660
    • Gennari, C.1
  • 7
    • 11844259698 scopus 로고    scopus 로고
    • Wiley-VCH-Verlag GmbH & Co.: Germany
    • (f) Mahrwald, R. Modern Aldol Reactions: Wiley-VCH-Verlag GmbH & Co.: Germany, 2004; Vol. 1 and 2.
    • (2004) Modern Aldol Reactions , vol.1-2
    • Mahrwald, R.1
  • 12
    • 0035905368 scopus 로고    scopus 로고
    • Recent examples of the enantioselective aldehyde cross-aldol reaction producing unprotected hydroxy aldehydes: (a) Denmark, S. E.; Ghosh, S. K. Angew. Chem., Int. Ed. 2001, 40, 4759
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 4759
    • Denmark, S.E.1    Ghosh, S.K.2
  • 14
    • 28044459433 scopus 로고    scopus 로고
    • (c) During the review process, an acetaldehyde Mukaiyama aldol reaction with aromatic aldehydes was reported: Denmark, S. E., Bui T. J. Org. Chem. 2005, 70, 10190.
    • (2005) J. Org. Chem. , vol.70 , pp. 10190
    • Denmark, S.E.1    Bui, T.2
  • 20
    • 30744463695 scopus 로고    scopus 로고
    • and references therein
    • (b) Mathieu, B.; Ghosez, L. Tetrahedron 2002, 58, 8210 and references therein.
    • (2002) Tetrahedron , vol.58 , pp. 8210
    • Mathieu, B.1    Ghosez, L.2
  • 21
    • 30744465022 scopus 로고    scopus 로고
    • note
    • For derivatization and single-crystal X-ray analysis or comparison to known compounds see Supporting Information.
  • 23
    • 30744474382 scopus 로고    scopus 로고
    • note
    • 1H NMR. The major product was isolated in the yield given in Table 2. The minor diastereomers were formed in small amounts and were not isolable in quantitities needed for structure elucidation.
  • 24
    • 30744458026 scopus 로고    scopus 로고
    • note
    • The chelation control results of this system will be studied and reported in due course.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.