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Volumn 5, Issue 16, 2003, Pages 2907-2909

β-nitro xanthates as olefin precursors

Author keywords

[No Author keywords available]

Indexed keywords

1,2 DICHLOROETHANE; ALKENE DERIVATIVE; NITRO DERIVATIVE; PEROXIDE; XANTHIC ACID DERIVATIVE;

EID: 0141743558     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol035027c     Document Type: Article
Times cited : (28)

References (15)
  • 3
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    • Ono, N.; Miyake, H.; Tamura, R.; Kaji, A. Tetrahedron Lett. 1981, 18, 1705. Ono, N.; Miyake, H.; Kamimura, A. Tetrahedron 1985, 41, 4013.
    • (1985) Tetrahedron , vol.41 , pp. 4013
    • Ono, N.1    Miyake, H.2    Kamimura, A.3
  • 5
    • 0001264691 scopus 로고    scopus 로고
    • Barton, D. H. R.; Jaszberenyi, J. Cs.; Tachdjian, C. Tetrahedron Lett. 1991, 32, 2703. For a similar application see: Kobertz, W. R.; Bertozzi, C. R.; Bednarski, N. D. J. Org. Chem. 1996, 61, 1894.
    • (1996) J. Org. Chem. , vol.61 , pp. 1894
    • Kobertz, W.R.1    Bertozzi, C.R.2    Bednarski, N.D.3
  • 6
    • 0000111727 scopus 로고    scopus 로고
    • Yao, C.-H.; Chu, C.-M.; Liu, J.-T. J. Org. Chem. 1998, 63, 719. Liu, J.-T.; Yao, C.-F. Tetrahedron Lett. 2001, 42, 6147. Liu, J.-T.; Jang, Y.-J.; Shih, Y.-K.; Hu, S.-R.; Chu, C.-M.; Yao, C.-F. J. Org. Chem. 2001, 66, 6021.
    • (1998) J. Org. Chem. , vol.63 , pp. 719
    • Yao, C.-H.1    Chu, C.-M.2    Liu, J.-T.3
  • 7
    • 0035959474 scopus 로고    scopus 로고
    • Yao, C.-H.; Chu, C.-M.; Liu, J.-T. J. Org. Chem. 1998, 63, 719. Liu, J.-T.; Yao, C.-F. Tetrahedron Lett. 2001, 42, 6147. Liu, J.-T.; Jang, Y.-J.; Shih, Y.-K.; Hu, S.-R.; Chu, C.-M.; Yao, C.-F. J. Org. Chem. 2001, 66, 6021.
    • (2001) Tetrahedron Lett. , vol.42 , pp. 6147
    • Liu, J.-T.1    Yao, C.-F.2
  • 9
    • 0030802574 scopus 로고    scopus 로고
    • For reviews see: Zard, S. Z. Angew. Chem., Int. Ed. Engl. 1997, 36, 672. Zard, S. Z. In Radicals in Organic Synthesis; Renaud, P., Sibi, M. P., Eds.; Wiley-VCH: Weinheim, Germany, 2001; Vol. 1, pp 90-108.
    • (1997) Angew. Chem., Int. Ed. Engl. , vol.36 , pp. 672
    • Zard, S.Z.1
  • 10
    • 0003123493 scopus 로고    scopus 로고
    • Renaud, P., Sibi, M. P., Eds.; Wiley-VCH: Weinheim, Germany
    • For reviews see: Zard, S. Z. Angew. Chem., Int. Ed. Engl. 1997, 36, 672. Zard, S. Z. In Radicals in Organic Synthesis; Renaud, P., Sibi, M. P., Eds.; Wiley-VCH: Weinheim, Germany, 2001; Vol. 1, pp 90-108.
    • (2001) Radicals in Organic Synthesis , vol.1 , pp. 90-108
    • Zard, S.Z.1
  • 12
    • 0000248247 scopus 로고
    • Nitro olefins 1 were either commercillay available or synthesized according to the classical Knœvenagel reaction: Jones, G. Org. React. 1967, 15, 204-599.
    • (1967) Org. React. , vol.15 , pp. 204-599
    • Jones, G.1
  • 14
    • 12044259240 scopus 로고    scopus 로고
    • For general reviews on this chemistry see: (a) Barrett, A. G. M. Chem. Soc. Rev. 1991, 20, 95. (b) Ono, N. The Nitro Group in Organic Synthesis; Wiley-VCH: Weinheim, Germany, 2001.
    • (1991) Chem. Soc. Rev. , vol.20 , pp. 95
    • Barrett, A.G.M.1
  • 15
    • 12044259240 scopus 로고    scopus 로고
    • Wiley-VCH: Weinheim, Germany
    • For general reviews on this chemistry see: (a) Barrett, A. G. M. Chem. Soc. Rev. 1991, 20, 95. (b) Ono, N. The Nitro Group in Organic Synthesis; Wiley-VCH: Weinheim, Germany, 2001.
    • (2001) The Nitro Group in Organic Synthesis
    • Ono, N.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.