메뉴 건너뛰기




Volumn 15, Issue 17, 2013, Pages 4516-4519

Dinuclear zinc-ProPhenol-catalyzed enantioselective α-hydroxyacetate aldol reaction with activated ester equivalents

Author keywords

[No Author keywords available]

Indexed keywords

3-HYDROXYBUTANAL; ALCOHOL DERIVATIVE; ALDEHYDE; ALDOL; ESTER; FUSED HETEROCYCLIC RINGS; KETONE; LACTONE; PELORUSIDE A; PYRROLE DERIVATIVE; ZINC;

EID: 84883827076     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol402081p     Document Type: Article
Times cited : (33)

References (39)
  • 2
    • 77951529935 scopus 로고    scopus 로고
    • For a review of direct aldol reactions, which includes α-hydroxyacetate aldols, see: Trost, B. M.; Brindle, C. S. Chem. Soc. Rev. 2010, 39, 1600-1632
    • (2010) Chem. Soc. Rev. , vol.39 , pp. 1600-1632
    • Trost, B.M.1    Brindle, C.S.2
  • 3
    • 79954533009 scopus 로고    scopus 로고
    • For a recent review on additions to imines, which includes α-hydroxycarbonyl enolate donors, see: Kobayashi, S.; Mori, Y.; Fossey, J. S.; Salter, M. M. Chem. Rev. 2011, 111, 2626-2704
    • (2011) Chem. Rev. , vol.111 , pp. 2626-2704
    • Kobayashi, S.1    Mori, Y.2    Fossey, J.S.3    Salter, M.M.4
  • 15
    • 77953041832 scopus 로고    scopus 로고
    • For an enantioselective direct aldol reaction with ester derivatives, see: Misaki, T.; Takimoto, G.; Sugimura, T. J. Am. Chem. Soc. 2010, 132, 6286-6287 and references therein
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 6286-6287
    • Misaki, T.1    Takimoto, G.2    Sugimura, T.3
  • 18
    • 0003417469 scopus 로고
    • Trost, B. M. Fleming, I. Pergamon Press: New York, Vol. Chapter 2.4.
    • Gennari, C. In Comprehensive Organic Synthesis; Trost, B. M.; Fleming, I., Eds.; Pergamon Press: New York, 1991; Vol. 2, Chapter 2.4.
    • (1991) Comprehensive Organic Synthesis , vol.2
    • Gennari, C.1
  • 20
    • 0003445429 scopus 로고    scopus 로고
    • Jacobsen, E. N. Pfaltz, A. Yamamoto, H. Springer: Heidelberg, Vol. Chapter 29.1.
    • Carreira, E. M. In Comprehensive Asymmetric Catalysis; Jacobsen, E. N.; Pfaltz, A.; Yamamoto, H., Eds.; Springer: Heidelberg, 1999; Vol. 3, Chapter 29.1.
    • (1999) Comprehensive Asymmetric Catalysis , vol.3
    • Carreira, E.M.1
  • 39
    • 42149187130 scopus 로고    scopus 로고
    • The absolute configuration of the diol products was confirmed by comparison of the optical rotation of 5a to reported values and then by analogy. See: Neisius, N. M.; Plietker, B. J. Org. Chem. 2008, 73, 3218-3227
    • (2008) J. Org. Chem. , vol.73 , pp. 3218-3227
    • Neisius, N.M.1    Plietker, B.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.