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Volumn 611, Issue 1-2, 2000, Pages 488-493

The reaction of 1,2,3-selenadiazole with olefins

Author keywords

1,2,3 selenadiazole; Dihydroselenophene; Olefins; Thermolysis

Indexed keywords


EID: 0001143840     PISSN: 0022328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-328X(00)00484-8     Document Type: Article
Times cited : (14)

References (37)
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    • For recent reviews on the synthesis and the utilization of 1,2,3-selenadiazoles, see: (a) W. Ando, N. Tokitoh, Heteroatom Chem. (1991) 1. (b) R. Tanaka, I. Shinkai, Prog. Heterocyclic Chem. 4 (1992) 123. D.H. Reid, in: R.C.S. Torr (Ed.), Comprehensive Heterocyclic Chemistry II: A Review of the Literature 1982-1995, vol. 4, Pergamon, Oxford, 1996, pp. 743-777. M. Regitz, S. Krill, Phosphorous Sulfur Silicon Relat. Elem. 15 (1996) 99. (e) N.I. Zmitrovich, M.L. Petrov, Zh. Org. Khim. 32 (1996) 1870. (f) V. Padmavathi, R.P. Sumathi, R.M.V. Ramana, R.D. Bhaskar, Org. Prep. Proced. Int. 30 (1998) 187 and refs. therein.
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    • For recent reviews on the synthesis and the utilization of 1,2,3-selenadiazoles, see: (a) W. Ando, N. Tokitoh, Heteroatom Chem. (1991) 1. (b) R. Tanaka, I. Shinkai, Prog. Heterocyclic Chem. 4 (1992) 123. D.H. Reid, in: R.C.S. Torr (Ed.), Comprehensive Heterocyclic Chemistry II: A Review of the Literature 1982-1995, vol. 4, Pergamon, Oxford, 1996, pp. 743-777. M. Regitz, S. Krill, Phosphorous Sulfur Silicon Relat. Elem. 15 (1996) 99. (e) N.I. Zmitrovich, M.L. Petrov, Zh. Org. Khim. 32 (1996) 1870. (f) V. Padmavathi, R.P. Sumathi, R.M.V. Ramana, R.D. Bhaskar, Org. Prep. Proced. Int. 30 (1998) 187 and refs. therein.
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    • R.C.S. Torr (Ed.), Pergamon, Oxford
    • For recent reviews on the synthesis and the utilization of 1,2,3-selenadiazoles, see: (a) W. Ando, N. Tokitoh, Heteroatom Chem. (1991) 1. (b) R. Tanaka, I. Shinkai, Prog. Heterocyclic Chem. 4 (1992) 123. D.H. Reid, in: R.C.S. Torr (Ed.), Comprehensive Heterocyclic Chemistry II: A Review of the Literature 1982-1995, vol. 4, Pergamon, Oxford, 1996, pp. 743-777. M. Regitz, S. Krill, Phosphorous Sulfur Silicon Relat. Elem. 15 (1996) 99. (e) N.I. Zmitrovich, M.L. Petrov, Zh. Org. Khim. 32 (1996) 1870. (f) V. Padmavathi, R.P. Sumathi, R.M.V. Ramana, R.D. Bhaskar, Org. Prep. Proced. Int. 30 (1998) 187 and refs. therein.
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    • For recent reviews on the synthesis and the utilization of 1,2,3-selenadiazoles, see: (a) W. Ando, N. Tokitoh, Heteroatom Chem. (1991) 1. (b) R. Tanaka, I. Shinkai, Prog. Heterocyclic Chem. 4 (1992) 123. D.H. Reid, in: R.C.S. Torr (Ed.), Comprehensive Heterocyclic Chemistry II: A Review of the Literature 1982-1995, vol. 4, Pergamon, Oxford, 1996, pp. 743-777. M. Regitz, S. Krill, Phosphorous Sulfur Silicon Relat. Elem. 15 (1996) 99. (e) N.I. Zmitrovich, M.L. Petrov, Zh. Org. Khim. 32 (1996) 1870. (f) V. Padmavathi, R.P. Sumathi, R.M.V. Ramana, R.D. Bhaskar, Org. Prep. Proced. Int. 30 (1998) 187 and refs. therein.
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    • For recent reviews on the synthesis and the utilization of 1,2,3-selenadiazoles, see: (a) W. Ando, N. Tokitoh, Heteroatom Chem. (1991) 1. (b) R. Tanaka, I. Shinkai, Prog. Heterocyclic Chem. 4 (1992) 123. D.H. Reid, in: R.C.S. Torr (Ed.), Comprehensive Heterocyclic Chemistry II: A Review of the Literature 1982-1995, vol. 4, Pergamon, Oxford, 1996, pp. 743-777. M. Regitz, S. Krill, Phosphorous Sulfur Silicon Relat. Elem. 15 (1996) 99. (e) N.I. Zmitrovich, M.L. Petrov, Zh. Org. Khim. 32 (1996) 1870. (f) V. Padmavathi, R.P. Sumathi, R.M.V. Ramana, R.D. Bhaskar, Org. Prep. Proced. Int. 30 (1998) 187 and refs. therein.
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    • Recently, there have been some reports on the synthesis of organometallic compounds by the reaction of various organometallic compounds with 1,2,3-selenadiazoles see: (a) W.C.P. Morley, Organometallics 8 (1989) 800. (b) M.R.J. Dorrity, A. Lavery, J.F. Malone, C.P. Morley, R.R. Vaughan, Heteroatom Chem. 3 (1992) 87. C.P. Morley, R.R. Vaughan, J. Chem. Soc. Dalton Trans. (1993) 703. C.P. Morley, R.R. Vaughan, J. Organomet. Chem. 444 (1993) 219. (e) P.K. Khanna, C.P. Morley, J. Chem. Res. (s) (1995) 64. (f) S, Ford, C.P. Morley, M.D. Vaira, Chem. Commun. (1998) 1305.
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    • Recently, there have been some reports on the synthesis of organometallic compounds by the reaction of various organometallic compounds with 1,2,3-selenadiazoles see: (a) W.C.P. Morley, Organometallics 8 (1989) 800. (b) M.R.J. Dorrity, A. Lavery, J.F. Malone, C.P. Morley, R.R. Vaughan, Heteroatom Chem. 3 (1992) 87. C.P. Morley, R.R. Vaughan, J. Chem. Soc. Dalton Trans. (1993) 703. C.P. Morley, R.R. Vaughan, J. Organomet. Chem. 444 (1993) 219. (e) P.K. Khanna, C.P. Morley, J. Chem. Res. (s) (1995) 64. (f) S, Ford, C.P. Morley, M.D. Vaira, Chem. Commun. (1998) 1305.
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    • Recently, there have been some reports on the synthesis of organometallic compounds by the reaction of various organometallic compounds with 1,2,3-selenadiazoles see: (a) W.C.P. Morley, Organometallics 8 (1989) 800. (b) M.R.J. Dorrity, A. Lavery, J.F. Malone, C.P. Morley, R.R. Vaughan, Heteroatom Chem. 3 (1992) 87. C.P. Morley, R.R. Vaughan, J. Chem. Soc. Dalton Trans. (1993) 703. C.P. Morley, R.R. Vaughan, J. Organomet. Chem. 444 (1993) 219. (e) P.K. Khanna, C.P. Morley, J. Chem. Res. (s) (1995) 64. (f) S, Ford, C.P. Morley, M.D. Vaira, Chem. Commun. (1998) 1305.
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    • 21844476549 scopus 로고
    • Recently, there have been some reports on the synthesis of organometallic compounds by the reaction of various organometallic compounds with 1,2,3-selenadiazoles see: (a) W.C.P. Morley, Organometallics 8 (1989) 800. (b) M.R.J. Dorrity, A. Lavery, J.F. Malone, C.P. Morley, R.R. Vaughan, Heteroatom Chem. 3 (1992) 87. C.P. Morley, R.R. Vaughan, J. Chem. Soc. Dalton Trans. (1993) 703. C.P. Morley, R.R. Vaughan, J. Organomet. Chem. 444 (1993) 219. (e) P.K. Khanna, C.P. Morley, J. Chem. Res. (s) (1995) 64. (f) S, Ford, C.P. Morley, M.D. Vaira, Chem. Commun. (1998) 1305.
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    • Morley, C.P.1    Vaughan, R.R.2
  • 11
    • 0000870594 scopus 로고
    • Recently, there have been some reports on the synthesis of organometallic compounds by the reaction of various organometallic compounds with 1,2,3-selenadiazoles see: (a) W.C.P. Morley, Organometallics 8 (1989) 800. (b) M.R.J. Dorrity, A. Lavery, J.F. Malone, C.P. Morley, R.R. Vaughan, Heteroatom Chem. 3 (1992) 87. C.P. Morley, R.R. Vaughan, J. Chem. Soc. Dalton Trans. (1993) 703. C.P. Morley, R.R. Vaughan, J. Organomet. Chem. 444 (1993) 219. (e) P.K. Khanna, C.P. Morley, J. Chem. Res. (s) (1995) 64. (f) S, Ford, C.P. Morley, M.D. Vaira, Chem. Commun. (1998) 1305.
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    • Khanna, P.K.1    Morley, C.P.2
  • 12
    • 0009594027 scopus 로고    scopus 로고
    • Recently, there have been some reports on the synthesis of organometallic compounds by the reaction of various organometallic compounds with 1,2,3-selenadiazoles see: (a) W.C.P. Morley, Organometallics 8 (1989) 800. (b) M.R.J. Dorrity, A. Lavery, J.F. Malone, C.P. Morley, R.R. Vaughan, Heteroatom Chem. 3 (1992) 87. C.P. Morley, R.R. Vaughan, J. Chem. Soc. Dalton Trans. (1993) 703. C.P. Morley, R.R. Vaughan, J. Organomet. Chem. 444 (1993) 219. (e) P.K. Khanna, C.P. Morley, J. Chem. Res. (s) (1995) 64. (f) S, Ford, C.P. Morley, M.D. Vaira, Chem. Commun. (1998) 1305.
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    • note
    • It has already been disclosed that 1,4-diselenine and selenophene derivatives were formed in the reaction of 1,2,3-selenadiazoles fused to a ring that is smaller than eight-membered under pyrolysis; see ref. [6].


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.