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Volumn 104, Issue 5, 2004, Pages 2239-2258

Synthesis of phosphorus and sulfur heterocycles via ring-closing olefin metathesis

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSTS; CHEMICAL BONDS; OLEFINS; PHOSPHORUS COMPOUNDS; SULFUR COMPOUNDS; SYNTHESIS (CHEMICAL);

EID: 2942609172     PISSN: 00092665     EISSN: None     Source Type: Journal    
DOI: 10.1021/cr020109k     Document Type: Article
Times cited : (625)

References (164)
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    • For examples of phosphorus compounds as pharmaceuticals, see: (a) Kafarski, P.; Lejczak, B. Curr. Med. Chem. 2001, 1, 301.
    • (2001) Curr. Med. Chem. , vol.1 , pp. 301
    • Kafarski, P.1    Lejczak, B.2
  • 46
    • 0034720908 scopus 로고    scopus 로고
    • For a paper containing several useful references on biologically and synthetically relevant sulfonamides, see: Dauben, P.; Dodd, R. H. Org. Lett. 2000, 2, 2327.
    • (2000) Org. Lett. , vol.2 , pp. 2327
    • Dauben, P.1    Dodd, R.H.2
  • 55
    • 0031838597 scopus 로고    scopus 로고
    • (a) Drugs Future 1998, 23, 365.
    • (1998) Drugs Future , vol.23 , pp. 365
  • 62
    • 2942532676 scopus 로고
    • Patai, S., Rappoport, Z., Eds.; Wiley Interscience: New York; Chapter 19.
    • (a) The Chemistry of Sulphonic Acids, Esters and Derivatives; Patai, S., Rappoport, Z., Eds.; Wiley Interscience: New York, 1991; Chapter 19.
    • (1991) The Chemistry of Sulphonic Acids, Esters and Derivatives
  • 75
    • 1442360753 scopus 로고    scopus 로고
    • Grubbs, R. H., Ed; Wiley-VCH: Weinheim
    • Handbook of Metathesis; Grubbs, R. H., Ed; Wiley-VCH: Weinheim, 2003.
    • (2003) Handbook of Metathesis
  • 92
    • 0034246704 scopus 로고    scopus 로고
    • (c) Yet, L. Chem. Rev. 2000, 100, 2963.
    • (2000) Chem. Rev. , vol.100 , pp. 2963
    • Yet, L.1
  • 145
  • 147
    • 0002497098 scopus 로고
    • In Patai, S., Rappaport, Z., Eds. Wiley: New York
    • (b) Buglass, A. J.; Tillet, J. G. In Patai, S., Rappaport, Z., Eds. Wiley: New York, 1991; p 789.
    • (1991) , pp. 789
    • Buglass, A.J.1    Tillet, J.G.2
  • 162
    • 0034685294 scopus 로고    scopus 로고
    • Allylic alcohol 51.2 can be readily derived from the condensation of trimethyl sulfonium ylide with (R)-benzyl-protected glycidol. Davoille, R. J.; Rutherford, D. T.; Christie, S. D. R. Tetrahedron Lett. 2000, 41, 1255.
    • (2000) Tetrahedron Lett. , vol.41 , pp. 1255
    • Davoille, R.J.1    Rutherford, D.T.2    Christie, S.D.R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.