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Volumn 11, Issue 14, 2005, Pages 4121-4131

Efficient solid-phase synthesis of peptide-based phosphine ligands: Towards combinatorial libraries of selective transition metal catalysts

Author keywords

Allylic compounds; Asymmetric catalysis; Peptides; Phosphine ligands; Solid phase synthesis

Indexed keywords

CATALYSIS; CHEMICAL VAPOR DEPOSITION; MATHEMATICAL MODELS; MOLECULAR BEAM EPITAXY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; QUANTUM THEORY; RAMAN SPECTROSCOPY; SEMICONDUCTOR MATERIALS; SPECTROSCOPIC ANALYSIS; SYNTHESIS (CHEMICAL);

EID: 22044452183     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/chem.200500105     Document Type: Article
Times cited : (45)

References (70)
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    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 4244-4247
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  • 57
    • 22044431517 scopus 로고    scopus 로고
    • note
    • 1H NMR data of all ligand precursor peptide scaffolds and oxidised peptide-based phosphine ligands.
  • 68
    • 0032515009 scopus 로고    scopus 로고
    • The base-system used was a mixture of N,O-bis(trimethylsilyl)acetamide (BSA) and tetrabutylammonium fluoride (TBAF), conditions developed by Gilbertson and co-workers, see: S. R. Gilbertson, C.-W. T. Chang, J. Org. Chem. 1998, 63, 8424-8431.
    • (1998) J. Org. Chem. , vol.63 , pp. 8424-8431
    • Gilbertson, S.R.1    Chang, C.-W.T.2
  • 70
    • 22044453731 scopus 로고    scopus 로고
    • note
    • At the NMR time-scale a plurality of conformers of building block 14 were present, resulting in broadening and splitting of peaks, due to the very bulky substituents.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.