메뉴 건너뛰기




Volumn 16, Issue 21, 2005, Pages 3536-3561

Synthesis of a novel class of chiral N,N,N-tridentate pyridinebisimidazoline ligands and their application in Ru-catalyzed asymmetric epoxidations

Author keywords

[No Author keywords available]

Indexed keywords

2,6 BIS(1 ACETYL 4,5 DIPHENYL 4,5 DIHYDRO 1H IMIDAZOL 2 YL)PYRIDINE; 2,6 BIS(1 ADAMANTOYL 4,5 DIPHENYL 4,5 DIHYDRO 1H IMIDAZOL 2 YL)PYRIDINE; 2,6 BIS(1 BENZOYL 4,5 DIPHENYL 4,5 DIHYDRO 1H IMIDAZOL 2 YL)PYRIDINE; 2,6 BIS(1 NAPHTHOYL 4,5 DIPHENYL 4,5 DIHYDRO 1H IMIDAZOL 2 YL)PYRIDINE; 2,6 BIS(1 PENTANOYL 4,5 DIPHENYL 4,5 DIHYDRO 1H IMIDAZOL 2 YL)PYRIDINE; 2,6 BIS(1 PHENYLACETYL 4,5 DIPHENYL 4,5 DIHYDRO 1H IMIDAZOL 2 YL)PYRIDINE; 2,6 BIS(2 NAPHTHOYL 4,5 DIPHENYL 4,5 DIHYDRO 1H IMIDAZOL 2 YL)PYRIDINE; 2,6 BIS[1 (2 METHYLBENZOYL) 4,5 DIPHENYL 4,5 DIHYDRO 1H IMIDAZOL 2 YL]PYRIDINE; 2,6 BIS[1 (2 METHYLPROPANOYL) 4,5 DIPHENYL 4,5 DIHYDRO 1H IMIDAZOL 2 YL]PYRIDINE; 2,6 BIS[1 (2,4,6 TRIMETHOXYBENZOYL) 4,5 DIPHENYL 4,5 DIHYDRO 1H IMIDAZOL 2 YL]PYRIDINE; 2,6 BIS[1 (2,6 DIMETHOXYBENZOYL) 4,5 DIPHENYL 4,5 DIHYDRO 1H IMIDAZOL 2 YL]PYRIDINE; 2,6 BIS[1 (3 METHYLBUTANOYL) 4,5 DIPHENYL 4,5 DIHYDRO 1H IMIDAZOL 2 YL]PYRIDINE; 2,6 BIS[1 (3,3 DIMETHYLBUTANOYL) 4,5 DIPHENYL 4,5 DIHYDRO 1H IMIDAZOL 2 YL]PYRIDINE; 2,6 BIS[1 (3,5 DI TERT BUTYLBENZOYL) 4,5 DIPHENYL 4,5 DIHYDRO 1H IMIDAZOL 2 YL]PYRIDINE; 2,6 BIS[1 (4 METHOXYBENZOYL) 4,5 DIPHENYL 4,5 DIHYDRO 1H IMIDAZOL 2 YL]PYRIDINE; 2,6 BIS[1 (4 TRIFLUOROMETHYLBENZOYL) 4,5 DIPHENYL 4,5 DIHYDRO 1H IMIDAZOL 2 YL]PYRIDINE; 2,6 BIS[1 (DIPHENYLACETYL) 4,5 DIPHENYL 4,5 DIHYDRO 1H IMIDAZOL 2 YL]PYRIDINE; 2,6 BIS[1 (PHENOXYCARBONYL) 4,5 DIPHENYL 4,5 DIHYDRO 1H IMIDAZOL 2 YL]PYRIDINE; 2,6 BIS[1 [2 (2 ISOPROPYL 5 METHYL)CYCLOHEXYLOXYACETYL] 4,5 DIPHENYL 4,5 DIHYDRO 1H IMIDAZOL 2 YL]PYRIDINE; 2,6 BIS[1 [2 (6 METHOXYNAPHTHALEN 2 YL)PROPIONYL] 4,5 DIPHENYL 4,5 DIHYDRO 1H IMIDAZOL 2 YL]PYRIDINE; ALKENE DERIVATIVE; AROMATIC COMPOUND; HYDROGEN PEROXIDE; IMIDAZOLINE DERIVATIVE; LIGAND; OXIDIZING AGENT; PYRIDINE DERIVATIVE; RUTHENIUM; RUTHENIUM DERIVATIVE; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 27944500694     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2005.08.060     Document Type: Article
Times cited : (54)

References (62)
  • 1
    • 0004219526 scopus 로고
    • A.N. Collins G.N. Sheldrake J. Crosby John Wiley Chichester
    • J. Crosby A.N. Collins G.N. Sheldrake J. Crosby Chirality in Industry 1992 John Wiley Chichester 1 66
    • (1992) Chirality in Industry , pp. 1-66
    • Crosby, J.1
  • 19
    • 0035742298 scopus 로고    scopus 로고
    • For a discussion on the 'ideal catalyst', see: J.A. Gladysz Pure Appl. Chem. 73 2001 1319 1324
    • (2001) Pure Appl. Chem. , vol.73 , pp. 1319-1324
    • Gladysz, J.A.1
  • 27
    • 3242857105 scopus 로고
    • For catalysis using pybox ligands see: A. Pfaltz Acc. Chem. Res. 26 1993 339 345
    • (1993) Acc. Chem. Res. , vol.26 , pp. 339-345
    • Pfaltz, A.1
  • 40
    • 27944456488 scopus 로고    scopus 로고
    • See experimental section for procedure.
    • See experimental section for procedure.
  • 41
    • 0030572020 scopus 로고    scopus 로고
    • For the synthesis of a diamide from aliphatic isocyanate using catalytic dibutyltindilaurate, see: B. Pugin J. Mol. Catal. A 107 1996 273 279
    • (1996) J. Mol. Catal. A , vol.107 , pp. 273-279
    • Pugin, B.1
  • 45
    • 0037958282 scopus 로고
    • For a review on Ru complexes in epoxidation reactions, see: G.A. Barf, and R.A. Sheldon J. Mol. Catal. 102 1995 23 39
    • (1995) J. Mol. Catal. , vol.102 , pp. 23-39
    • Barf, G.A.1    Sheldon, R.A.2
  • 46
    • 0042649931 scopus 로고    scopus 로고
    • for recent achievements in Ru-based epoxidations with different oxidants, see: N. End, and A. Pfaltz Chem. Commun. 1999 589 590
    • (1999) Chem. Commun. , pp. 589-590
    • End, N.1    Pfaltz, A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.