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Volumn 66, Issue 21, 2010, Pages 3814-3823

Formation of chiral tertiary homoallylic alcohols via Evans aldol reaction or enzymatic resolution and their influence on the Sharpless asymmetric dihydroxylation

Author keywords

Asymmetric synthesis; Enzymatic resolution; Homoallylic alcohols; Lipases; Sharpless asymmetric dihydroxylation

Indexed keywords

(2 METHOXYPENT 4 EN 2 YL)BENZENE; 1 METHOXY 4 ((2 PHENYLPENT 4 EN 2 YLOXY)METHYL) BENZENE; 2 PHENYLPENT 4 EN 2 OL; ACETOPHENONE; ALCOHOL DERIVATIVE; TERT BUTYLDIMETHYL(2 PHENYLPENT 4 EN 2 YLOXY)SILANE; UNCLASSIFIED DRUG;

EID: 77951145314     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2010.03.048     Document Type: Article
Times cited : (14)

References (97)
  • 1
    • 77951129843 scopus 로고    scopus 로고
    • Reviews
    • Reviews:
  • 19
  • 41
  • 42
    • 77951135835 scopus 로고    scopus 로고
    • Reviews
    • Reviews:
  • 48
    • 28644442668 scopus 로고    scopus 로고
    • Jacobsen E.N., Pfaltz A., and Yamamoto H. (Eds), Springer-Verlag, Heidelberg Supplement 2, pp 21-42
    • Bayer A. In: Jacobsen E.N., Pfaltz A., and Yamamoto H. (Eds). Comprehensive Asymmetric Catalysis (2004), Springer-Verlag, Heidelberg Supplement 2, pp 21-42
    • (2004) Comprehensive Asymmetric Catalysis
    • Bayer, A.1
  • 59
    • 77951104048 scopus 로고    scopus 로고
    • Selected examples
    • Selected examples:
  • 96
    • 77951117782 scopus 로고    scopus 로고
    • note
    • In order to allow convenient comparison of the NMR data of the triols 3 with those of the PMP-acetals 9, the numbering scheme indicated in Scheme 7 (and used throughout the text and experimental part) is different from the IUPAC nomenclature. The correct IUPAC numbering and -naming of 9 is: 2-(4-methoxyphenyl)-6-methyl-6-phenyl-1,3-dioxan-4-yl)methanol.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.