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Volumn 13, Issue 5, 2011, Pages 1230-1233

Transfer of Chirality by the Use of an All Carbon Tether

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EID: 79952138343     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol2001182     Document Type: Article
Times cited : (10)

References (51)
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    • For a recent discussion of the synthesis of eudesmanes, see
    • For a recent discussion of the synthesis of eudesmanes, see: Chen, K.; Baran, P. S. Nature 2009, 459, 824
    • (2009) Nature , vol.459 , pp. 824
    • Chen, K.1    Baran, P.S.2
  • 4
    • 79952171232 scopus 로고    scopus 로고
    • For recent reviews on enantioselective Diels-Alder reactions, see:;; Direct Book Publishing.
    • For recent reviews on enantioselective Diels-Alder reactions, see: Corey, E. J.; Kürti, L. Enantioselective Chemical Synthesis; Direct Book Publishing: 2010.
    • (2010) Enantioselective Chemical Synthesis
    • Corey, E.J.1    Kürti, L.2
  • 5
    • 61949362917 scopus 로고    scopus 로고
    • references cited therein
    • Corey, E. J. Angew. Chem., Int. Ed. 2009, 48, 2100 and references cited therein
    • (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 2100
    • Corey, E.J.1
  • 24
    • 0030802574 scopus 로고    scopus 로고
    • For reviews of the xanthate transfer chemistry
    • For reviews of the xanthate transfer chemistry, see: Zard, S. Z. Angew. Chem., Int. Ed. 1997, 36, 672
    • (1997) Angew. Chem., Int. Ed. , vol.36 , pp. 672
    • Zard, S.Z.1
  • 25
    • 0003123493 scopus 로고    scopus 로고
    • Renaud, P.; Sibi, M. P., Eds.; Wiley-VCH: Weinheim
    • Zard, S. Z. In Radicals in Organic Synthesis; Renaud, P.; Sibi, M. P., Eds.; Wiley-VCH: Weinheim, 2001; Vol. 1, p 90.
    • (2001) Radicals in Organic Synthesis , vol.1 , pp. 90
    • Zard, S.Z.1
  • 43
    • 78650843633 scopus 로고    scopus 로고
    • Barner-Kowollik, C., Ed.; Wiley-VCH: Weinheim
    • Zard, S. Z. In Handbook of RAFT Polymerization; Barner-Kowollik, C., Ed.; Wiley-VCH: Weinheim, 2008; pp 151 -187.
    • (2008) Handbook of RAFT Polymerization , pp. 151-187
    • Zard, S.Z.1
  • 45
    • 79952145056 scopus 로고    scopus 로고
    • It is interesting to note in this respect that ozonolysis of the olefin in compound 32 would also give a propionaldehyde side chain that could condense with the acetonitrile moiety, but this time to give a cis -decalin.
    • It is interesting to note in this respect that ozonolysis of the olefin in compound 32 would also give a propionaldehyde side chain that could condense with the acetonitrile moiety, but this time to give a cis -decalin.
  • 46
    • 0342285086 scopus 로고
    • The addition of the ethoxyvinyllithium to ketone 44 is surprisingly stereoselective. The addition of isopropylmagnesium iodide to the corresponding aldehyde has been reported and appears to give only one epimer, but no comments are given by the authors
    • The addition of the ethoxyvinyllithium to ketone 44 is surprisingly stereoselective. The addition of isopropylmagnesium iodide to the corresponding aldehyde has been reported and appears to give only one epimer, but no comments are given by the authors: Nakazaki, M.; Naemura, K.; Kondo, Y. J. Org. Chem. 1976, 41, 1229
    • (1976) J. Org. Chem. , vol.41 , pp. 1229
    • Nakazaki, M.1    Naemura, K.2    Kondo, Y.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.