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Volumn 71, Issue 17, 2006, Pages 6497-6507

Solid phase approaches to N-heterocycles using a sulfur linker cleaved by SmI2

Author keywords

[No Author keywords available]

Indexed keywords

HECK REACTION; LINKER SYSTEM; MICHAEL CYCLIZATION; SOLID PHASE;

EID: 33747387589     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo060940n     Document Type: Article
Times cited : (51)

References (56)
  • 1
    • 0033574590 scopus 로고    scopus 로고
    • For recent reviews on linkers and cleavage strategies for solid-phase organic synthesis: (a) James, I. W. Tetrahedron 1999, 55, 4855.
    • (1999) Tetrahedron , vol.55 , pp. 4855
    • James, I.W.1
  • 4
    • 0001948147 scopus 로고
    • For reviews on the use of samarium(II) iodide in organic synthesis: (a) Soderquist, J. A. Aldrichimica Acta 1991, 24, 15.
    • (1991) Aldrichimica Acta , vol.24 , pp. 15
    • Soderquist, J.A.1
  • 29
    • 2942576049 scopus 로고    scopus 로고
    • For recent reviews on the Pummerer reaction see (a) Bur, S. K.; Padwa, A. Chem. Rev. 2004, 104, 2401.
    • (2004) Chem. Rev. , vol.104 , pp. 2401
    • Bur, S.K.1    Padwa, A.2
  • 38
    • 33747404550 scopus 로고    scopus 로고
    • note
    • For the preparation of a different thiol resin via a thiourea, see ref 9a.
  • 39
    • 33747395818 scopus 로고    scopus 로고
    • note
    • -1) is presumably due to oxidative cross-linking of the thiol functional groups (See Experimental Section).
  • 44
    • 33747419570 scopus 로고    scopus 로고
    • note
    • See Supporting Information for the X-ray structure of the major isomer of 7 (CCDC 601447).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.