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Volumn 47, Issue 51, 2006, Pages 9067-9071

Organocatalyzed asymmetric α-hydroxyamination of α-branched aldehydes: asymmetric synthesis of optically active N-protected α,α-disubstituted amino aldehydes and amino alcohols

Author keywords

Aminoxylation; Asymmetric catalysis; Hydroxyamination; Organocatalysis

Indexed keywords

ALDEHYDE DERIVATIVE; AMINOALCOHOL; NITROSOBENZENE; PROLINE; TETRAZOLE DERIVATIVE;

EID: 33750942375     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.10.081     Document Type: Article
Times cited : (39)

References (41)
  • 1
    • 0037241493 scopus 로고    scopus 로고
    • For selected reviews, see:
    • For selected reviews, see:. Weinreb S.M. Acc. Chem. Res. 36 (2003) 59-65
    • (2003) Acc. Chem. Res. , vol.36 , pp. 59-65
    • Weinreb, S.M.1
  • 13
    • 0035886887 scopus 로고    scopus 로고
    • For general reviews on organocatalysis, see:
    • For general reviews on organocatalysis, see:. Dalko P.I., and Moisan L. Angew. Chem., Int. Ed. 40 (2001) 3726-3748
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 3726-3748
    • Dalko, P.I.1    Moisan, L.2
  • 14
    • 4143094833 scopus 로고    scopus 로고
    • Special issue: Asymmetric Organocatalysis. Acc. Chem. Res. 37 (2004) 487-631
    • (2004) Acc. Chem. Res. , vol.37 , pp. 487-631
  • 17
    • 0037043180 scopus 로고    scopus 로고
    • For reviews of proline-catalyzed asymmetric synthesis, see: 5573-5590
    • For reviews of proline-catalyzed asymmetric synthesis, see:. List B. Tetrahedron 58 (2002) 5573-5590
    • (2002) Tetrahedron , vol.58
    • List, B.1
  • 30
    • 33645454252 scopus 로고    scopus 로고
    • During the course of this study, Gong and co-workers reported a prolinamide catalyzed α-hydroxyamination reaction of α-methyl aldehydes. A moderated enantioselectivity (up to 64% ee) was given in that case:
    • During the course of this study, Gong and co-workers reported a prolinamide catalyzed α-hydroxyamination reaction of α-methyl aldehydes. A moderated enantioselectivity (up to 64% ee) was given in that case:. Guo H.-M., Cheng L., Cun L.-F., Gong L.-Z., Mi A.-Q., and Jiang Y.-Z. Chem. Commun. (2006) 429-431
    • (2006) Chem. Commun. , pp. 429-431
    • Guo, H.-M.1    Cheng, L.2    Cun, L.-F.3    Gong, L.-Z.4    Mi, A.-Q.5    Jiang, Y.-Z.6
  • 40
    • 33750961180 scopus 로고    scopus 로고
    • note
    • + 292.1566, found 292.1570.
  • 41
    • 33750934527 scopus 로고    scopus 로고
    • note
    • major = 48.9 min, 42% ee.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.