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Volumn 75, Issue 22, 2010, Pages 7809-7821

Development of the Ireland-Claisen rearrangement of alkoxy- and aryloxy-substituted allyl glycinates

Author keywords

[No Author keywords available]

Indexed keywords

ACID SYSTEMS; ARYLOXY; CLAISEN REARRANGEMENT; DIASTEREOSELECTIVITIES; DIRECT ACCESS; IRELAND; SIGMATROPIC REARRANGEMENTS;

EID: 78449245405     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo1017124     Document Type: Article
Times cited : (17)

References (110)
  • 1
    • 0036882394 scopus 로고    scopus 로고
    • For a review concerning mechanism and specificity, see
    • For a review concerning mechanism and specificity, see: Hedstrom, L. Chem. Rev. 2002, 102, 4501-4523
    • (2002) Chem. Rev. , vol.102 , pp. 4501-4523
    • Hedstrom, L.1
  • 20
    • 33744805367 scopus 로고    scopus 로고
    • For selected recent synthetic approaches, see
    • For selected recent synthetic approaches, see: Balskus, E. P.; Jacobsen, E. N. J. Am. Chem. Soc. 2006, 128, 6810-6812
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 6810-6812
    • Balskus, E.P.1    Jacobsen, E.N.2
  • 65
    • 33847030354 scopus 로고    scopus 로고
    • For recent aldol approaches to β-hydroxy α-amino acids, see
    • For recent aldol approaches to β-hydroxy α-amino acids, see: Ma, B.; Parkinson, J. L.; Castle, S. L. Tetrahedron Lett. 2007, 48, 2083-2086
    • (2007) Tetrahedron Lett. , vol.48 , pp. 2083-2086
    • Ma, B.1    Parkinson, J.L.2    Castle, S.L.3
  • 95
    • 0020696324 scopus 로고
    • For retro aldol and elimination occurring on attempted O -alkylation, see
    • For retro aldol and elimination occurring on attempted O -alkylation, see: Barlos, K.; Papaioannou, D.; Cordopatis, P.; Theodoropoulos, D. Tetrahedron 1983, 39, 475-478
    • (1983) Tetrahedron , vol.39 , pp. 475-478
    • Barlos, K.1    Papaioannou, D.2    Cordopatis, P.3    Theodoropoulos, D.4
  • 97
    • 3843094836 scopus 로고    scopus 로고
    • For retro aldol during aldol formation of β-hydroxy α-amino acids, see
    • For retro aldol during aldol formation of β-hydroxy α-amino acids, see: Ooi, T.; Kameda, M.; Taniguchi, M.; Maruoka, K. J. Am. Chem. Soc. 2004, 126, 9685-9694
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 9685-9694
    • Ooi, T.1    Kameda, M.2    Taniguchi, M.3    Maruoka, K.4
  • 101
    • 4344610661 scopus 로고    scopus 로고
    • For recent reviews concerning the Ireland-Claisen rearrangement, see
    • For recent reviews concerning the Ireland-Claisen rearrangement, see: Castro, A. M. M. Chem. Rev. 2004, 104, 2939
    • (2004) Chem. Rev. , vol.104 , pp. 2939
    • Castro, A.M.M.1
  • 105
    • 0035825096 scopus 로고    scopus 로고
    • In contrast to oxygen substitution at C-3 of ester 6 in the allyl unit, silicon substitution at C-3 and rearrangement is a fruitful method for forming allyl silane amino acids; see
    • In contrast to oxygen substitution at C-3 of ester 6 in the allyl unit, silicon substitution at C-3 and rearrangement is a fruitful method for forming allyl silane amino acids; see: Mohamed, M.; Brook, M. A. Tetrahedron Lett. 2001, 42, 191-193
    • (2001) Tetrahedron Lett. , vol.42 , pp. 191-193
    • Mohamed, M.1    Brook, M.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.