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Volumn 80, Issue 10, 2003, Pages 923-925

Regiospecific conversion of substituted cinnamic acids to cinnamyl alcohols

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL; BORON; CARBON; CHLORINE; CINNAMIC ACID; CINNAMYL ALCOHOL; HYDROGEN; OXYGEN; SODIUM;

EID: 1842711967     PISSN: 00194522     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (1)

References (18)
  • 2
    • 1542478596 scopus 로고
    • J. Mitra and A. K. Mitra, J. Chem. Soc., Perkin Trans. I, 1992, 1285; Indian J. Chem., Sect. B, 1992, 31, 452; 1994, 33, 953.
    • (1992) Indian J. Chem., Sect. B , vol.31 , pp. 452
  • 3
    • 1842739179 scopus 로고
    • J. Mitra and A. K. Mitra, J. Chem. Soc., Perkin Trans. I, 1992, 1285; Indian J. Chem., Sect. B, 1992, 31, 452; 1994, 33, 953.
    • (1994) Indian J. Chem., Sect. B , vol.33 , pp. 953
  • 4
    • 0003543593 scopus 로고
    • VCH, New York
    • R. C. Larock, "Comprehensive Organic Transformations", VCH, New York, 1989; K. Soai, S. Yokoyama and K. Mochida, Synthesis, 1987, 647; A. Giannis and K. Sandhoff, Angew. Chem. Int. Ed. Engl., 1989, 28, 218; J. Das and S. Chandrasekaran, Synth. Commun., 1990, 20, 911; Y. Suseela and M. Periasamy, Tetrahedron, 1992, 48, 371.
    • (1989) Comprehensive Organic Transformations
    • Larock, R.C.1
  • 5
    • 85082673916 scopus 로고
    • R. C. Larock, "Comprehensive Organic Transformations", VCH, New York, 1989; K. Soai, S. Yokoyama and K. Mochida, Synthesis, 1987, 647; A. Giannis and K. Sandhoff, Angew. Chem. Int. Ed. Engl., 1989, 28, 218; J. Das and S. Chandrasekaran, Synth. Commun., 1990, 20, 911; Y. Suseela and M. Periasamy, Tetrahedron, 1992, 48, 371.
    • (1987) Synthesis , pp. 647
    • Soai, K.1    Yokoyama, S.2    Mochida, K.3
  • 6
    • 84990101204 scopus 로고
    • R. C. Larock, "Comprehensive Organic Transformations", VCH, New York, 1989; K. Soai, S. Yokoyama and K. Mochida, Synthesis, 1987, 647; A. Giannis and K. Sandhoff, Angew. Chem. Int. Ed. Engl., 1989, 28, 218; J. Das and S. Chandrasekaran, Synth. Commun., 1990, 20, 911; Y. Suseela and M. Periasamy, Tetrahedron, 1992, 48, 371.
    • (1989) Angew. Chem. Int. Ed. Engl. , vol.28 , pp. 218
    • Giannis, A.1    Sandhoff, K.2
  • 7
    • 1842739178 scopus 로고
    • R. C. Larock, "Comprehensive Organic Transformations", VCH, New York, 1989; K. Soai, S. Yokoyama and K. Mochida, Synthesis, 1987, 647; A. Giannis and K. Sandhoff, Angew. Chem. Int. Ed. Engl., 1989, 28, 218; J. Das and S. Chandrasekaran, Synth. Commun., 1990, 20, 911; Y. Suseela and M. Periasamy, Tetrahedron, 1992, 48, 371.
    • (1990) Synth. Commun. , vol.20 , pp. 911
    • Das, J.1    Chandrasekaran, S.2
  • 8
    • 0026592562 scopus 로고
    • R. C. Larock, "Comprehensive Organic Transformations", VCH, New York, 1989; K. Soai, S. Yokoyama and K. Mochida, Synthesis, 1987, 647; A. Giannis and K. Sandhoff, Angew. Chem. Int. Ed. Engl., 1989, 28, 218; J. Das and S. Chandrasekaran, Synth. Commun., 1990, 20, 911; Y. Suseela and M. Periasamy, Tetrahedron, 1992, 48, 371.
    • (1992) Tetrahedron , vol.48 , pp. 371
    • Suseela, Y.1    Periasamy, M.2
  • 14
    • 1842638301 scopus 로고    scopus 로고
    • note
    • Refs. 5 and 7 reported that the same amount of saturated alcohol was also produced.
  • 17
    • 85008039425 scopus 로고
    • 4 have been used earlier to reduce cinnamic acid having no substitution to cinnamyl alcohol (K. Ishizumi, K. Koga and S. Yamada, Chem. Pharm. Bull., 1968, 16, 492). On utilising their reaction condition, we got an appreciable amount of saturated alcohol from cinnamic acid.
    • (1968) Chem. Pharm. Bull. , vol.16 , pp. 492
    • Ishizumi, K.1    Koga, K.2    Yamada, S.3
  • 18
    • 85105829668 scopus 로고    scopus 로고
    • note
    • 2Et were used and phenolic-OH group has been converted to carbonate derivative.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.