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Volumn 28, Issue 11, 1998, Pages 1989-2000

Incorporation of two molecules of carbon monoxide into N-lithioketimine leading to azetidine-2,3-diones

Author keywords

[No Author keywords available]

Indexed keywords

AZETIDINE DERIVATIVE; CARBON MONOXIDE; HETEROCYCLIC COMPOUND;

EID: 0031839014     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1080/00397919808007173     Document Type: Article
Times cited : (7)

References (47)
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    • Some alkynes are known to undergo formal [2+1+1]cycloaddition with two molecules of carbon monoxide leading to cyclobutene-2,3-dione derivatives in the presense of transition-metal carbonyl complexes. (a) Radhakrishnan, U.; Periasamy, M. Organometallics 1997, 16, 1800. (b) Periasamy, M.; Radhakrishnan, U.; Brunet, J. -J.; Chauvin, R.; ElZaizi, A. W. Chem. Commun. 1996, 1499. (c) Herrera, A.; Hoberg, H.; Mynott, R. J. Organomet. Chem. 1981, 222, 331. (d) Herrera, A.; Hoberg, H. Synthesis 1981, 831. (e) Hoberg, H.; Herrera, A. Angew. Chem., Int. Ed. Engl. 1980, 19, 927.
    • (1997) Organometallics , vol.16 , pp. 1800
    • Radhakrishnan, U.1    Periasamy, M.2
  • 15
    • 0342361244 scopus 로고    scopus 로고
    • Some alkynes are known to undergo formal [2+1+1]cycloaddition with two molecules of carbon monoxide leading to cyclobutene-2,3-dione derivatives in the presense of transition-metal carbonyl complexes. (a) Radhakrishnan, U.; Periasamy, M. Organometallics 1997, 16, 1800. (b) Periasamy, M.; Radhakrishnan, U.; Brunet, J. -J.; Chauvin, R.; ElZaizi, A. W. Chem. Commun. 1996, 1499. (c) Herrera, A.; Hoberg, H.; Mynott, R. J. Organomet. Chem. 1981, 222, 331. (d) Herrera, A.; Hoberg, H. Synthesis 1981, 831. (e) Hoberg, H.; Herrera, A. Angew. Chem., Int. Ed. Engl. 1980, 19, 927.
    • (1996) Chem. Commun. , pp. 1499
    • Periasamy, M.1    Radhakrishnan, U.2    Brunet, J.J.3    Chauvin, R.4    Elzaizi, A.W.5
  • 16
    • 0348019902 scopus 로고
    • Some alkynes are known to undergo formal [2+1+1]cycloaddition with two molecules of carbon monoxide leading to cyclobutene-2,3-dione derivatives in the presense of transition-metal carbonyl complexes. (a) Radhakrishnan, U.; Periasamy, M. Organometallics 1997, 16, 1800. (b) Periasamy, M.; Radhakrishnan, U.; Brunet, J. -J.; Chauvin, R.; ElZaizi, A. W. Chem. Commun. 1996, 1499. (c) Herrera, A.; Hoberg, H.; Mynott, R. J. Organomet. Chem. 1981, 222, 331. (d) Herrera, A.; Hoberg, H. Synthesis 1981, 831. (e) Hoberg, H.; Herrera, A. Angew. Chem., Int. Ed. Engl. 1980, 19, 927.
    • (1981) Organomet. Chem. , vol.222 , pp. 331
    • Herrera, A.1    Hoberg, H.2    Mynott, R.J.3
  • 17
    • 84988062745 scopus 로고
    • Some alkynes are known to undergo formal [2+1+1]cycloaddition with two molecules of carbon monoxide leading to cyclobutene-2,3-dione derivatives in the presense of transition-metal carbonyl complexes. (a) Radhakrishnan, U.; Periasamy, M. Organometallics 1997, 16, 1800. (b) Periasamy, M.; Radhakrishnan, U.; Brunet, J. -J.; Chauvin, R.; ElZaizi, A. W. Chem. Commun. 1996, 1499. (c) Herrera, A.; Hoberg, H.; Mynott, R. J. Organomet. Chem. 1981, 222, 331. (d) Herrera, A.; Hoberg, H. Synthesis 1981, 831. (e) Hoberg, H.; Herrera, A. Angew. Chem., Int. Ed. Engl. 1980, 19, 927.
    • (1981) Synthesis , pp. 831
    • Herrera, A.1    Hoberg, H.2
  • 18
    • 84985579881 scopus 로고
    • Some alkynes are known to undergo formal [2+1+1]cycloaddition with two molecules of carbon monoxide leading to cyclobutene-2,3-dione derivatives in the presense of transition-metal carbonyl complexes. (a) Radhakrishnan, U.; Periasamy, M. Organometallics 1997, 16, 1800. (b) Periasamy, M.; Radhakrishnan, U.; Brunet, J. -J.; Chauvin, R.; ElZaizi, A. W. Chem. Commun. 1996, 1499. (c) Herrera, A.; Hoberg, H.; Mynott, R. J. Organomet. Chem. 1981, 222, 331. (d) Herrera, A.; Hoberg, H. Synthesis 1981, 831. (e) Hoberg, H.; Herrera, A. Angew. Chem., Int. Ed. Engl. 1980, 19, 927.
    • (1980) Angew. Chem., Int. Ed. Engl. , vol.19 , pp. 927
    • Hoberg, H.1    Herrera, A.2
  • 37
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    • Ito, Y.; Matsuura, T.; Nishimura, S.; Ishikawa, M. Tetrahedron Lett. 1986, 27, 3261. See, however, Jutzi, P.; Schröder, F. -W. J. Organomet. Chem. 1970, 24, C43.
    • (1970) J. Organomet. Chem. , vol.24
    • Jutzi, P.1    Schröder, F.W.2
  • 42
    • 2642663419 scopus 로고    scopus 로고
    • A reviewer has suggested the possibility of electrocyclic ring closure. All these alternatives must wait for futher study. (Equation Presented)
    • A reviewer has suggested the possibility of electrocyclic ring closure. All these alternatives must wait for futher study. (Equation Presented)
  • 45
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    • Eur. Pat. Appl. EP 144885, 1985
    • Franz, M.; Wolfgang, S. Eur. Pat. Appl. EP 144885, 1985; Chem. Abstr. 1985, 104, 33778.
    • Franz, M.1    Wolfgang, S.2
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    • Franz, M.; Wolfgang, S. Eur. Pat. Appl. EP 144885, 1985; Chem. Abstr. 1985, 104, 33778.
    • (1985) Chem. Abstr. , vol.104 , pp. 33778


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.