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Volumn 46, Issue 3, 2009, Pages 447-454

Suzuki-Miyaura arylations of tetramic acid sulfonates: Evaluation of lactam protection, sulfonate esters, and sterics

Author keywords

[No Author keywords available]

Indexed keywords

LACTAM; SULFONIC ACID DERIVATIVE; TETRAMIC ACID DERIVATIVE; TOLUENESULFONIC ACID DERIVATIVE; TRIFLUOROMETHANESULFONIC ACID;

EID: 66349128871     PISSN: 0022152X     EISSN: None     Source Type: Journal    
DOI: 10.1002/jhet.96     Document Type: Article
Times cited : (10)

References (52)
  • 19
    • 66349099796 scopus 로고    scopus 로고
    • After our entry into this field (ref. 11b), the preparation of 4-aryl-3-pyrrolin-2-ones was reported by Albrecht and Bach using a Negishi cross-coupling reaction of 4-bromo-3-pyrrolin-2-ones (ref. 7)
    • After our entry into this field (ref. 11b), the preparation of 4-aryl-3-pyrrolin-2-ones was reported by Albrecht and Bach using a Negishi cross-coupling reaction of 4-bromo-3-pyrrolin-2-ones (ref. 7).
  • 26
    • 1242270584 scopus 로고    scopus 로고
    • One example of a Stille cross-coupling reaction of 4-stannyl- 3-pyrrolin-2-ones was reported
    • One example of a Stille cross-coupling reaction of 4-stannyl- 3-pyrrolin-2-ones was reported: Santos, M. M. M.; Lobo, A. M.; Prabhakar, S.; Marques, M. M. B. Tetrahedron Lett 2004, 45, 2347.
    • (2004) Tetrahedron Lett , vol.45 , pp. 2347
    • Santos, M.M.M.1    Lobo, A.M.2    Prabhakar, S.3    Marques, M.M.B.4
  • 28
    • 32244446189 scopus 로고    scopus 로고
    • An allylic amine, prepared via a four-component reaction involving an allenylboronate, proved to be a useful precursor to a 1-benzyl-4-aryl-3- pyrrolin-2-one
    • An allylic amine, prepared via a four-component reaction involving an allenylboronate, proved to be a useful precursor to a 1-benzyl-4-aryl-3- pyrrolin-2-one: Tonogaki, K.; Itami, K.; Yoshida, J.-I. J Am Chem Soc 2006, 128, 1464.
    • (2006) J Am Chem Soc , vol.128 , pp. 1464
    • Tonogaki, K.1    Itami, K.2    Yoshida, J.-I.3
  • 30
  • 40
    • 0344256186 scopus 로고
    • Dieckmann cyclocondensations leading to 3-aryltetramic acids
    • Dieckmann cyclocondensations leading to 3-aryltetramic acids: (a) King, J. A.; McMillan, F. H. J Am Chem Soc 1950, 72, 1236;
    • (1950) J Am Chem Soc , vol.72 , pp. 1236
    • King, J.A.1    McMillan, F.H.2
  • 50
    • 33751317736 scopus 로고    scopus 로고
    • Review of synthesis without protecting groups
    • Review of synthesis without protecting groups: Hoffmann, R. W. Synthesis 2006, 3531.
    • (2006) Synthesis , pp. 3531
    • Hoffmann, R.W.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.