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Volumn 6, Issue C, 2005, Pages 415-436

Chapter 13 Functionalization of pyridines and thiazoles via the halogen-dance reaction, application to the total synthesis of caerulomycin c and WS75624 B

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EID: 34548703001     PISSN: 18746004     EISSN: None     Source Type: Book Series    
DOI: 10.1016/S1874-6004(05)80036-X     Document Type: Article
Times cited : (5)

References (61)
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    • (1996) Comprehensive heterocyclic Chemistry II , vol.5 , pp. 37
    • Comins, D.L.1    Joseph, S.P.2
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    • Nucleophilic aromatic substitution at the 3- or 5-position of pyridines is known to be more difficult than at the 2- or 4-position. see, Plenum, New York
    • Nucleophilic aromatic substitution at the 3- or 5-position of pyridines is known to be more difficult than at the 2- or 4-position. see. Schofield K. Hetero-Aromatic Nitrogen Compounds Pyrroles and Pyridines (1967), Plenum, New York 244
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    • 3, Cul, DMF, 80°C). See. Diederich F., and Stang P.J. (Eds), Wiley-VCH, New York
    • 3, Cul, DMF, 80°C). See. In: Diederich F., and Stang P.J. (Eds). Metal-catalyzed Cross-coupling Reactions (1998), Wiley-VCH, New York
    • (1998) Metal-catalyzed Cross-coupling Reactions
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    • For other examples of halogen dance reactions on thiophenes and furans, see
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    • For other examples where an in situ trapping with a silyl chloride proceeds faster than a halogen dance, see. 27.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.