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Volumn 127, Issue 34, 2005, Pages 11956-11957

A highly efficient and direct approach for synthesis of enantiopure β-amino alcohols by reductive cross-coupling of chiral N-tert- butanesulfinyl imines with aldehydes

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; AMINOALCOHOL; BENZALDEHYDE; CARBONYL DERIVATIVE; IMINE;

EID: 24144490041     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja054401w     Document Type: Article
Times cited : (121)

References (38)
  • 4
    • 0034697199 scopus 로고    scopus 로고
    • For reviews on the synthesis of β-amino alcohols, see: (a) Bergmeier, S. C. Tetrahedron 2000, 56, 2561.
    • (2000) Tetrahedron , vol.56 , pp. 2561
    • Bergmeier, S.C.1
  • 18
    • 0026753568 scopus 로고
    • For an example using chiral imine derived from (R)-phenylglycinol methyl ether to give moderate dr and ee, see: (j) Ito, H.; Taguchi, T.; Hanzawa, Y. Tetrahedron Lett. 1992, 33, 4469.
    • (1992) Tetrahedron Lett. , vol.33 , pp. 4469
    • Ito, H.1    Taguchi, T.2    Hanzawa, Y.3
  • 27
    • 33645593733 scopus 로고    scopus 로고
    • note
    • 1H NMR analysis of the crude material.
  • 28
    • 33645593454 scopus 로고    scopus 로고
    • note
    • Only 47% of the yield was achieved in the absence of 'BuOH.
  • 30
    • 33645589164 scopus 로고    scopus 로고
    • note
    • For X-ray structure and related data, see Supporting Information.
  • 32
    • 33645585643 scopus 로고    scopus 로고
    • note
    • A larger excess was used for its poor solubility in THF at -78 °C.
  • 33
    • 33645602755 scopus 로고    scopus 로고
    • note
    • Yield based on recovered starting material.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.