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Volumn 14, Issue 12, 2012, Pages 3068-3071

Sulfinyl-mediated stereoselective overman rearrangements and Diels-Alder cycloadditions

Author keywords

[No Author keywords available]

Indexed keywords

DRUG DERIVATIVE; SAFROLE; SULFOXIDE; SULFUR DERIVATIVE;

EID: 84862524617     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol301139a     Document Type: Article
Times cited : (20)

References (66)
  • 7
  • 50
    • 0027527467 scopus 로고
    • Lithiation and trapping with aldehydes leads to the substrates of this study 2 / 3. In most cases 2 and 3 are readily interconverted by a Mitsunobu protocol
    • Craig, D.; Daniels, K.; MacKenzie, A. R. Tetrahedron 1993, 49, 11263-11304. Lithiation and trapping with aldehydes leads to the substrates of this study 2 / 3. In most cases 2 and 3 are readily interconverted by a Mitsunobu protocol
    • (1993) Tetrahedron , vol.49 , pp. 11263-11304
    • Craig, D.1    Daniels, K.2    MacKenzie, A.R.3
  • 55
    • 77954547147 scopus 로고    scopus 로고
    • The relative configuration of final products 6 and 8 was assigned from their Z geometry (NOE), the relative configuration of the starting materials, and the accepted mechanism for the Overman rearrangement
    • Lee, S. I.; Moon, S. Y.; Hwang, G.-S.; Ryu, D. H. Org. Lett. 2010, 12, 3234-3237. The relative configuration of final products 6 and 8 was assigned from their Z geometry (NOE), the relative configuration of the starting materials, and the accepted mechanism for the Overman rearrangement
    • (2010) Org. Lett. , vol.12 , pp. 3234-3237
    • Lee, S.I.1    Moon, S.Y.2    Hwang, G.-S.3    Ryu, D.H.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.