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Volumn , Issue 8, 2006, Pages 1255-1259

Synthesis of 4-nitrophenyl sulfones and application in the modified Julia olefination

Author keywords

4 nitrophenyl sulfone; Alkene; Nucleophilic aromatic substitution; Olefination; Smiles rearrangement

Indexed keywords

4 FLUORONITROBENZENE DERIVATIVE; 4 NITROPHENYL SULFONE DERIVATIVE; ALDEHYDE; CARBONYL DERIVATIVE; CINNAMIC ACID; NITROBENZENE DERIVATIVE; STILBENE DERIVATIVE; STYRENE DERIVATIVE; SULFONE DERIVATIVE; THIOL; UNCLASSIFIED DRUG;

EID: 33744487140     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-939682     Document Type: Article
Times cited : (25)

References (51)
  • 13
    • 0037038993 scopus 로고    scopus 로고
    • For a recent review about the modified Julia olefination and its application in natural product syntheses, see: Blakemore, P. R. J. Chem. Soc., Perkin Trans. 1 2002, 2563.
    • (2002) J. Chem. Soc., Perkin Trans. 1 , pp. 2563
    • Blakemore, P.R.1
  • 15
    • 17944363137 scopus 로고    scopus 로고
    • Corrigendum
    • Corrigendum: Tetrahedron Lett. 2001, 42, 6619.
    • (2001) Tetrahedron Lett. , vol.42 , pp. 6619
  • 27
    • 33947339750 scopus 로고
    • All synthesized sulfones were employed in analytically pure manner, their data correspond to the literature, (a) Compound 1a: Bost, R. W.; Turner, J. O.; Norton, R. D. J. Am. Chem. Soc. 1932, 54, 1985.
    • (1932) J. Am. Chem. Soc. , vol.54 , pp. 1985
    • Bost, R.W.1    Turner, J.O.2    Norton, R.D.3
  • 39
    • 33744497054 scopus 로고    scopus 로고
    • note
    • (i) For compound 2ca: analytical data correspond to a commercial sample.
  • 50
    • 33744482573 scopus 로고    scopus 로고
    • note
    • Yields and E/Z ratios of the modified Julia olefination with NP sulfones using KHMDS as base after flash chromatography for 2ba: 14% (97:3), 2bb: 55% (>99:1), 2bd: 33% (96:4), 2bg: 58% (95:5), 2ca: 23% (88:12), 2cb: 48% (52:48), 2cd: 32% (94:6), 2cg: 73% (59:41).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.