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Volumn 46, Issue 26, 2007, Pages 5011-5014

Tetraarylphosphonium salts as soluble supports for the synthesis of small molecules

Author keywords

Asymmetric synthesis; Chiral auxiliaries; Combinatorial chemistry; Peptides; Soluble supports

Indexed keywords

ASYMMETRIC SYNTHESIS; CHIRAL AUXILIARIES; COMBINATORIAL CHEMISTRY; PHOSPHONIUM SALTS; SOLID PHASE SYNTHESIS; SOLUBLE SUPPORTS;

EID: 34447325367     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200700833     Document Type: Article
Times cited : (36)

References (45)
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    • For recent reviews, see: a) A. R. Vaino, K. D. Janda, J. Comb. Chem. 2000, 2, 579;
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  • 12
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    • For a recent approach, see
    • For a recent approach, see: R. A. Houghten, Y. Yu, J. Am. Chem. Soc. 2005, 127, 8582.
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 8582
    • Houghten, R.A.1    Yu, Y.2
  • 13
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    • For pioneering work using a PEG support, see: a
    • For pioneering work using a PEG support, see: a) M. Mutter, H. Hagenmaier, E. Bayer, Angew. Chem. 1971, 83, 883;
    • (1971) Angew. Chem , vol.83 , pp. 883
    • Mutter, M.1    Hagenmaier, H.2    Bayer, E.3
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    • c) W. Zhang, Chem. Rev. 2004, 104, 2531.
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    • Zhang, W.1
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    • Angew. Chem. Int. Ed. 2006, 45, 1415.
    • (2006) Chem. Int. Ed , vol.45 , pp. 1415
    • Angew1
  • 41
    • 85008894386 scopus 로고    scopus 로고
    • To avoid the formation of diketopiperazinine, a dipeptide was directly coupled to the first phosphonium-supported amino acid in the second coupling step: E. Pedroso, A. Grandas, X. de las Heras, R. Eritja, E. Giralt, Tetrahedron Lett. 1986, 27, 743.
    • To avoid the formation of diketopiperazinine, a dipeptide was directly coupled to the first phosphonium-supported amino acid in the second coupling step: E. Pedroso, A. Grandas, X. de las Heras, R. Eritja, E. Giralt, Tetrahedron Lett. 1986, 27, 743.
  • 42
    • 34447321256 scopus 로고    scopus 로고
    • Formation of the amide bond occurred quantitatively. Although the presence of DIPEA and DIC was occasionally observed, no residual Fmoc amino acid could be detected liquid chromatography-MS
    • Formation of the amide bond occurred quantitatively. Although the presence of DIPEA and DIC was occasionally observed, no residual Fmoc amino acid could be detected (liquid chromatography-MS).
  • 43
    • 34447310496 scopus 로고    scopus 로고
    • See the Supporting Information for details
    • See the Supporting Information for details.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.