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Volumn 47, Issue 42, 2008, Pages 8120-8122

Fluorinating cleavage of solid phase linkers for combinatorial synthesis

Author keywords

Alkyl fluorides; Combinatorial chemistry; Dithiane linkers; Fluorination; Solid phase synthesis

Indexed keywords

BIOASSAY; BIOCHIPS; CHEMICAL REACTIONS; FLUORINATION; FLUORINE COMPOUNDS; HALOGENATION; MICROARRAYS; SULFUR;

EID: 54049122258     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200802126     Document Type: Article
Times cited : (12)

References (46)
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    • for a review: d
    • for a review: d) M. Shimizu, T. Hiyama, Angew. Chem. 2005, 117, 218-234;
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    • Shimizu, M.1    Hiyama, T.2
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    • (2006) Angew. Chem. Int. Ed , vol.45 , pp. 5432-5446
  • 25
    • 0000905921 scopus 로고    scopus 로고
    • There are a few linkers that can be cleaved by fluoride ions, but with none of these systems is fluorine introduced into the target structures. See e.g.: a R. Ramage, C. A. Barron, S. Bielecki, D.W. Thomas, Tetrahedron Lett. 1987, 28, 4105-4108;
    • There are a few linkers that can be cleaved by fluoride ions, but with none of these systems is fluorine introduced into the target structures. See e.g.: a) R. Ramage, C. A. Barron, S. Bielecki, D.W. Thomas, Tetrahedron Lett. 1987, 28, 4105-4108;
  • 28
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    • For an example of a photolabile dithiane linker, see
    • b) For an example of a photolabile dithiane linker, see: H. B. Lee, S. Balasubramanian, J. Org. Chem. 1999, 64, 3454-3460.
    • (1999) J. Org. Chem , vol.64 , pp. 3454-3460
    • Lee, H.B.1    Balasubramanian, S.2
  • 44
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    • For important organometallic reactions on solid supports see, e.g, c
    • For important organometallic reactions on solid supports see, e.g.: c) L. Boymond, M. Rottländer, G. Cahiez, P. Knochel, Angew. Chem. 1998, 110, 1801-1803;
    • (1998) Angew. Chem , vol.110 , pp. 1801-1803
    • Boymond, L.1    Rottländer, M.2    Cahiez, G.3    Knochel, P.4
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.