메뉴 건너뛰기




Volumn 47, Issue 36, 2008, Pages 6865-6868

Convergent preparation of enantiomerically pure polyalkylated cyclopropane derivatives

Author keywords

Alkylation; Asymmetric synthesis; Cyclopropane; Lithium

Indexed keywords

CHEMICAL REACTIONS;

EID: 52449130400     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200802093     Document Type: Article
Times cited : (31)

References (102)
  • 1
    • 0001043514 scopus 로고
    • For general reviews on cyclopropanes, see: a, Eds, S. Patai, Z. Rappoport, Wiley, New York
    • For general reviews on cyclopropanes, see: a) The Chemistry of the Cyclopropyl Group, Vol. 2 (Eds.: S. Patai, Z. Rappoport), Wiley, New York, 1995;
    • (1995) The Chemistry of the Cyclopropyl Group, Vol. 2
  • 8
    • 0027172932 scopus 로고
    • For reviews, see: a
    • For reviews, see: a) H. M. L. Davies, Tetrahedron 1993, 49, 5203;
    • (1993) Tetrahedron , vol.49 , pp. 5203
    • Davies, H.M.L.1
  • 11
    • 0001373505 scopus 로고
    • Eds, B. M. Trost, I. Fleming, Pergamon, Oxford
    • d) T. Hudlicky, J. Reed in Comprehensive Organic Synthesis, Vol. 5 (Eds.: B. M. Trost, I. Fleming), Pergamon, Oxford, 1991, p. 899;
    • (1991) Comprehensive Organic Synthesis , vol.5 , pp. 899
    • Hudlicky, T.1    Reed, J.2
  • 14
    • 0000531841 scopus 로고
    • For reviews on cyclopropane ring-opening reactions, see: a
    • For reviews on cyclopropane ring-opening reactions, see: a) D. C. Nonhebel, Chem. Soc. Rev. 1993, 22, 347;
    • (1993) Chem. Soc. Rev , vol.22 , pp. 347
    • Nonhebel, D.C.1
  • 18
    • 53249136038 scopus 로고    scopus 로고
    • For recent reviews, see: a Stereoselective Synthesis of Organic Compounds: H. U. Reissig in Methoden Org. Chem. (Houben-Weyl), 1995, p. 3179;
    • For recent reviews, see: a) "Stereoselective Synthesis of Organic Compounds": H. U. Reissig in Methoden Org. Chem. (Houben-Weyl), 1995, p. 3179;
  • 25
  • 30
    • 35048841685 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 7364-7376;
    • (2007) Angew. Chem. Int. Ed , vol.46 , pp. 7364-7376
  • 41
    • 0242659053 scopus 로고    scopus 로고
    • For recent reports of cyclopropanation of nonfunctionalized alkenes, see: a
    • For recent reports of cyclopropanation of nonfunctionalized alkenes, see: a) J. Long, Y. Yuan, Y. Shi, J. Am. Chem. Soc. 2003, 125, 13632;
    • (2003) J. Am. Chem. Soc , vol.125 , pp. 13632
    • Long, J.1    Yuan, Y.2    Shi, Y.3
  • 51
    • 4544330787 scopus 로고    scopus 로고
    • For sulfoxide/metal exchange, see: a
    • For sulfoxide/metal exchange, see: a) S. Farhat, I. Marek, Angew. Chem. 2002, 114, 1468;
    • (2002) Angew. Chem , vol.114 , pp. 1468
    • Farhat, S.1    Marek, I.2
  • 59
    • 0001318042 scopus 로고    scopus 로고
    • h) T. Satoh, Chem. Rev. 1996, 96, 3303;
    • (1996) Chem. Rev , vol.96 , pp. 3303
    • Satoh, T.1
  • 78
    • 53249139264 scopus 로고    scopus 로고
    • The reaction temperature and the amount of n-butyllithium used are critical for the success of the reaction. For analogous reactions on monosulfinyloxirane, see T. Satoh, Y. Kanedo, K. Yamakawa, Bull. Chem. Soc. Jpn. 1986, 59, 2463.
    • The reaction temperature and the amount of n-butyllithium used are critical for the success of the reaction. For analogous reactions on monosulfinyloxirane, see T. Satoh, Y. Kanedo, K. Yamakawa, Bull. Chem. Soc. Jpn. 1986, 59, 2463.
  • 95
    • 53249139909 scopus 로고    scopus 로고
    • Tertiary alkyllithium species (such as 8) are usually sluggish nucleophilic species, see: Organometallics in Synthesis, 2nd ed. (Ed..: M. Schlosser), Wiley, Chichester, 2002, p. 1.
    • Tertiary alkyllithium species (such as 8) are usually sluggish nucleophilic species, see: Organometallics in Synthesis, 2nd ed. (Ed..: M. Schlosser), Wiley, Chichester, 2002, p. 1.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.