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Volumn 12, Issue 21, 2010, Pages 4916-4919

Horner-wadsworth-emmons reagents as azomethine ylide analogues: Pyrrole synthesis via (3 + 2) cycloaddition

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EID: 78049516560     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol102075y     Document Type: Article
Times cited : (63)

References (53)
  • 12
    • 78049509744 scopus 로고    scopus 로고
    • For examples
    • For examples
  • 32
    • 78049521929 scopus 로고    scopus 로고
    • For other routes to Münchnones
    • For other routes to Münchnones
  • 47
    • 0027405466 scopus 로고
    • 5a also undergoes standard Wadsworth-Emmons reactions with aldehydes. See Supporting Information and
    • 5a also undergoes standard Wadsworth-Emmons reactions with aldehydes. See Supporting Information and: Couture, A.; Deniau, E.; Grandclaudon, P. Tetrahedron Lett. 1993, 34, 1479
    • (1993) Tetrahedron Lett. , vol.34 , pp. 1479
    • Couture, A.1    Deniau, E.2    Grandclaudon, P.3
  • 51
    • 78049489935 scopus 로고    scopus 로고
    • TMSCl is the formal byproduct of 7 formation with P(o -catechyl)OTMS; however, excess TMSCl is beneficial to the reaction (Table 2, entry 2 is in 37% yield without additional TMSCl)
    • TMSCl is the formal byproduct of 7 formation with P(o -catechyl)OTMS; however, excess TMSCl is beneficial to the reaction (Table 2, entry 2 is in 37% yield without additional TMSCl).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.