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Volumn , Issue 4, 1998, Pages 202-203

Cobalt(II) Chloride. Aluminium Promoted Allylation of Aldehydes with Allylic Halides

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EID: 2542499079     PISSN: 03082342     EISSN: None     Source Type: Journal    
DOI: 10.1039/a704607c     Document Type: Article
Times cited : (4)

References (27)
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    • For other catalytic reactions of cobalt(II) chloride see: J. Marquet and M. Moreno-Manas, Chem. Lett., 1981, 173; H. Matsuda and H. Kanai, Chem. Lett. 1981, 395; J. Iqbal, B. Bhatia and N. K. Nayyar, Chem. Rev., 1994 94, 519: M. Mukhopadhyay and J. Iqbal, J. Org. Chem., 1997, 62, 1843.
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    • For other catalytic reactions of cobalt(II) chloride see: J. Marquet and M. Moreno-Manas, Chem. Lett., 1981, 173; H. Matsuda and H. Kanai, Chem. Lett. 1981, 395; J. Iqbal, B. Bhatia and N. K. Nayyar, Chem. Rev., 1994 94, 519: M. Mukhopadhyay and J. Iqbal, J. Org. Chem., 1997, 62, 1843.
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    • For other catalytic reactions of cobalt(II) chloride see: J. Marquet and M. Moreno-Manas, Chem. Lett., 1981, 173; H. Matsuda and H. Kanai, Chem. Lett. 1981, 395; J. Iqbal, B. Bhatia and N. K. Nayyar, Chem. Rev., 1994 94, 519: M. Mukhopadhyay and J. Iqbal, J. Org. Chem., 1997, 62, 1843.
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    • 0001398838 scopus 로고    scopus 로고
    • For other catalytic reactions of cobalt(II) chloride see: J. Marquet and M. Moreno-Manas, Chem. Lett., 1981, 173; H. Matsuda and H. Kanai, Chem. Lett. 1981, 395; J. Iqbal, B. Bhatia and N. K. Nayyar, Chem. Rev., 1994 94, 519: M. Mukhopadhyay and J. Iqbal, J. Org. Chem., 1997, 62, 1843.
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    • Mukhopadhyay, M.1    Iqbal, J.2
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    • 0000698226 scopus 로고
    • Other similar allylation of carbonyl compounds in aqueous media has been reported to be a Borbier-type reaction: J. Nokami, I. Otera, T. Sudo and R. Okawara, Organometallics, 1983, 2, 191; C. Petrier, J. Eihorn and J. L. Luche, Tetrahedron Lett., 1985, 26, 1449; C. Petrer and J. L. Luche, J. Org. Chem., 1985, 50, 910; K. Uneyama, N. Karmaki, A. Moriya and S. Torri, J. Org. Chem., 1985, 50, 5396; K. Uneyama, H. Nambu and S. Torri, Tetrahedron Lett., 1986, 27, 2395; A. Yanagisawa, H. Inoue, M. Morodome and H. Yamamoto, J. Am. Chem. Soc. 1993, 115, 10 356; A. Lubineau J. Auge and Y. Queneau, Synthesis, 1994, 741; M. B. Isaac and T. H. Chan, Tetrahedron Lett., 1995, 36, 8957.
    • (1983) Organometallics , vol.2 , pp. 191
    • Nokami, J.1    Otera, I.2    Sudo, T.3    Okawara, R.4
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    • 0009569697 scopus 로고
    • Other similar allylation of carbonyl compounds in aqueous media has been reported to be a Borbier-type reaction: J. Nokami, I. Otera, T. Sudo and R. Okawara, Organometallics, 1983, 2, 191; C. Petrier, J. Eihorn and J. L. Luche, Tetrahedron Lett., 1985, 26, 1449; C. Petrer and J. L. Luche, J. Org. Chem., 1985, 50, 910; K. Uneyama, N. Karmaki, A. Moriya and S. Torri, J. Org. Chem., 1985, 50, 5396; K. Uneyama, H. Nambu and S. Torri, Tetrahedron Lett., 1986, 27, 2395; A. Yanagisawa, H. Inoue, M. Morodome and H. Yamamoto, J. Am. Chem. Soc. 1993, 115, 10 356; A. Lubineau J. Auge and Y. Queneau, Synthesis, 1994, 741; M. B. Isaac and T. H. Chan, Tetrahedron Lett., 1995, 36, 8957.
    • (1985) Tetrahedron Lett. , vol.26 , pp. 1449
    • Petrier, C.1    Eihorn, J.2    Luche, J.L.3
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    • 33845377368 scopus 로고
    • Other similar allylation of carbonyl compounds in aqueous media has been reported to be a Borbier-type reaction: J. Nokami, I. Otera, T. Sudo and R. Okawara, Organometallics, 1983, 2, 191; C. Petrier, J. Eihorn and J. L. Luche, Tetrahedron Lett., 1985, 26, 1449; C. Petrer and J. L. Luche, J. Org. Chem., 1985, 50, 910; K. Uneyama, N. Karmaki, A. Moriya and S. Torri, J. Org. Chem., 1985, 50, 5396; K. Uneyama, H. Nambu and S. Torri, Tetrahedron Lett., 1986, 27, 2395; A. Yanagisawa, H. Inoue, M. Morodome and H. Yamamoto, J. Am. Chem. Soc. 1993, 115, 10 356; A. Lubineau J. Auge and Y. Queneau, Synthesis, 1994, 741; M. B. Isaac and T. H. Chan, Tetrahedron Lett., 1995, 36, 8957.
    • (1985) J. Org. Chem. , vol.50 , pp. 910
    • Petrer, C.1    Luche, J.L.2
  • 15
    • 0001402171 scopus 로고
    • Other similar allylation of carbonyl compounds in aqueous media has been reported to be a Borbier-type reaction: J. Nokami, I. Otera, T. Sudo and R. Okawara, Organometallics, 1983, 2, 191; C. Petrier, J. Eihorn and J. L. Luche, Tetrahedron Lett., 1985, 26, 1449; C. Petrer and J. L. Luche, J. Org. Chem., 1985, 50, 910; K. Uneyama, N. Karmaki, A. Moriya and S. Torri, J. Org. Chem., 1985, 50, 5396; K. Uneyama, H. Nambu and S. Torri, Tetrahedron Lett., 1986, 27, 2395; A. Yanagisawa, H. Inoue, M. Morodome and H. Yamamoto, J. Am. Chem. Soc. 1993, 115, 10 356; A. Lubineau J. Auge and Y. Queneau, Synthesis, 1994, 741; M. B. Isaac and T. H. Chan, Tetrahedron Lett., 1995, 36, 8957.
    • (1985) J. Org. Chem. , vol.50 , pp. 5396
    • Uneyama, K.1    Karmaki, N.2    Moriya, A.3    Torri, S.4
  • 16
    • 46149137683 scopus 로고
    • Other similar allylation of carbonyl compounds in aqueous media has been reported to be a Borbier-type reaction: J. Nokami, I. Otera, T. Sudo and R. Okawara, Organometallics, 1983, 2, 191; C. Petrier, J. Eihorn and J. L. Luche, Tetrahedron Lett., 1985, 26, 1449; C. Petrer and J. L. Luche, J. Org. Chem., 1985, 50, 910; K. Uneyama, N. Karmaki, A. Moriya and S. Torri, J. Org. Chem., 1985, 50, 5396; K. Uneyama, H. Nambu and S. Torri, Tetrahedron Lett., 1986, 27, 2395; A. Yanagisawa, H. Inoue, M. Morodome and H. Yamamoto, J. Am. Chem. Soc. 1993, 115, 10 356; A. Lubineau J. Auge and Y. Queneau, Synthesis, 1994, 741; M. B. Isaac and T. H. Chan, Tetrahedron Lett., 1995, 36, 8957.
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    • Uneyama, K.1    Nambu, H.2    Torri, S.3
  • 17
    • 85010645580 scopus 로고
    • Other similar allylation of carbonyl compounds in aqueous media has been reported to be a Borbier-type reaction: J. Nokami, I. Otera, T. Sudo and R. Okawara, Organometallics, 1983, 2, 191; C. Petrier, J. Eihorn and J. L. Luche, Tetrahedron Lett., 1985, 26, 1449; C. Petrer and J. L. Luche, J. Org. Chem., 1985, 50, 910; K. Uneyama, N. Karmaki, A. Moriya and S. Torri, J. Org. Chem., 1985, 50, 5396; K. Uneyama, H. Nambu and S. Torri, Tetrahedron Lett., 1986, 27, 2395; A. Yanagisawa, H. Inoue, M. Morodome and H. Yamamoto, J. Am. Chem. Soc. 1993, 115, 10 356; A. Lubineau J. Auge and Y. Queneau, Synthesis, 1994, 741; M. B. Isaac and T. H. Chan, Tetrahedron Lett., 1995, 36, 8957.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 10356
    • Yanagisawa, A.1    Inoue, H.2    Morodome, M.3    Yamamoto, H.4
  • 18
    • 0027934153 scopus 로고
    • Other similar allylation of carbonyl compounds in aqueous media has been reported to be a Borbier-type reaction: J. Nokami, I. Otera, T. Sudo and R. Okawara, Organometallics, 1983, 2, 191; C. Petrier, J. Eihorn and J. L. Luche, Tetrahedron Lett., 1985, 26, 1449; C. Petrer and J. L. Luche, J. Org. Chem., 1985, 50, 910; K. Uneyama, N. Karmaki, A. Moriya and S. Torri, J. Org. Chem., 1985, 50, 5396; K. Uneyama, H. Nambu and S. Torri, Tetrahedron Lett., 1986, 27, 2395; A. Yanagisawa, H. Inoue, M. Morodome and H. Yamamoto, J. Am. Chem. Soc. 1993, 115, 10 356; A. Lubineau J. Auge and Y. Queneau, Synthesis, 1994, 741; M. B. Isaac and T. H. Chan, Tetrahedron Lett., 1995, 36, 8957.
    • (1994) Synthesis , pp. 741
    • Lubineau, A.1    Auge, J.2    Queneau, Y.3
  • 19
    • 0028818170 scopus 로고
    • Other similar allylation of carbonyl compounds in aqueous media has been reported to be a Borbier-type reaction: J. Nokami, I. Otera, T. Sudo and R. Okawara, Organometallics, 1983, 2, 191; C. Petrier, J. Eihorn and J. L. Luche, Tetrahedron Lett., 1985, 26, 1449; C. Petrer and J. L. Luche, J. Org. Chem., 1985, 50, 910; K. Uneyama, N. Karmaki, A. Moriya and S. Torri, J. Org. Chem., 1985, 50, 5396; K. Uneyama, H. Nambu and S. Torri, Tetrahedron Lett., 1986, 27, 2395; A. Yanagisawa, H. Inoue, M. Morodome and H. Yamamoto, J. Am. Chem. Soc. 1993, 115, 10 356; A. Lubineau J. Auge and Y. Queneau, Synthesis, 1994, 741; M. B. Isaac and T. H. Chan, Tetrahedron Lett., 1995, 36, 8957.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 8957
    • Isaac, M.B.1    Chan, T.H.2


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