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Volumn 70, Issue 24, 2005, Pages 10202-10205

Highly stereoselective synthesis of trisubstituted vinylcyclopropane derivatives via arsonium ylides

Author keywords

[No Author keywords available]

Indexed keywords

CATALYST SELECTIVITY; PROPANE; REACTION KINETICS; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

EID: 28044450399     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo051782n     Document Type: Article
Times cited : (27)

References (46)
  • 12
    • 0141853181 scopus 로고    scopus 로고
    • For cyclopropanation with a diazalkanes bearing two electron-withdrawing groups, see: (a) Wurz, R. P.; Charette, A. B. Org. Lett. 2003, 5, 2327.
    • (2003) Org. Lett. , vol.5 , pp. 2327
    • Wurz, R.P.1    Charette, A.B.2
  • 40
    • 9344269208 scopus 로고
    • Triphenylarsine
    • Paquette, L. A., Ed.; Wiley: New York
    • (f) Huang, Y.-Z.; Shi, L.-L.; Zhou, Z.-L. Triphenylarsine. In Encyclopedia of Reagents for Organic Synthesis; Paquette, L. A., Ed.; Wiley: New York, 1995; p 5339. The arsenic compounds described here should be handled with caution. Although triphenylarsine has been used for years as a ligand by inorganic chemists and seems to have only moderate acute toxicity. repeated exposure should be avoided by working with care in an efficient hood. Because the compounds described in this paper are nonvolatile, actual danger is minimal.
    • (1995) Encyclopedia of Reagents for Organic Synthesis , pp. 5339
    • Huang, Y.-Z.1    Shi, L.-L.2    Zhou, Z.-L.3
  • 41
    • 0009717830 scopus 로고
    • A similar "salt effect" was reported in the epoxidation of arsonium ylides, Still, W. C.; Novack, V. J. J. Am. Chem. Soc. 1981, 103, 1283.
    • (1981) J. Am. Chem. Soc. , vol.103 , pp. 1283
    • Still, W.C.1    Novack, V.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.