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Volumn 71, Issue 4, 2006, Pages 1626-1632

Diversity-oriented synthesis of 3-iodochromones and heteroatom analogues via ICl-induced cyclization

Author keywords

[No Author keywords available]

Indexed keywords

CYCLIZATION; DIVERSITY-ORIENTED SYNTHESIS; MOLECULAR COMPLEXITY; PALLADIUM-CATALYZED TRANSFORMATIONS;

EID: 33644499135     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0523722     Document Type: Article
Times cited : (158)

References (72)
  • 1
    • 33644839988 scopus 로고    scopus 로고
    • For diversity-oriented synthesis, see: Tan, D. S. Nature Chem. Biol. 2005, 1, 74.
    • (2005) Nature Chem. Biol. , vol.1 , pp. 74
    • Tan, D.S.1
  • 35
    • 0037155526 scopus 로고    scopus 로고
    • (b) Yue, D.; Larock, R. C. J. Org. Chem. 2002, 67, 1905.
    • (2002) , vol.67 , pp. 1905
  • 66
    • 33644555358 scopus 로고    scopus 로고
    • note
    • The starting material is fully recovered after the reaction. It is possible that the IC1 coordinates to the nitrogen moiety of the pyridine to form a pyridinium salt first, which makes the pyridine ring even more electron-deficient and unreactive.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.