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Volumn 52, Issue 20, 1996, Pages 7183-7200

Isothiazoles. Part VI.1 Cycloaddition of azides to isothiazole dioxides: Synthesis of thiadiazabicyclo[3.1.0]hexene derivatives and their thermal rearrangement to thiazete dioxides, 1,2,6-thiadiazine dioxides and pyrazoles

Author keywords

[No Author keywords available]

Indexed keywords

ISOTHIAZOLE DERIVATIVE; PYRAZOLE DERIVATIVE; THIADIAZINE DERIVATIVE;

EID: 0029967601     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4020(96)00336-5     Document Type: Article
Times cited : (20)

References (36)
  • 5
    • 0040975478 scopus 로고
    • Padwa, A.; Taylor, E. C.; Weissberger, A. Eds., John Wiley and Sons, Inc. New York
    • Huisgen, R. 1,3-Dipolar Cycloaddition Chemistry, Padwa, A.; Taylor, E. C.; Weissberger, A. Eds., John Wiley and Sons, Inc. New York, 1984; I, pp. 135-137; Houk, K. N.; Yamaguchi, K. ibid., II, pp. 443-444.
    • (1984) 1,3-Dipolar Cycloaddition Chemistry , vol.1 , pp. 135-137
    • Huisgen, R.1
  • 9
    • 0002045618 scopus 로고
    • Trost, B. M.; Fleming, I.; Paquette, L. A. Eds., Pergamon Press, Oxford, 2.2
    • Several examples of related transformations are well represented in: Ghosez, L.; Marchand Brynaert, J. Comprehensive Organic Synthesis Trost, B. M.; Fleming, I.; Paquette, L. A. Eds., Pergamon Press, Oxford, 1991, 2.2, pp. 85-123; Durst, T.; Breau, T. ibid., 6.1, pp.675-694; Okamura, W. H.; De Lera, A. ibid., 6.2, pp. 699-745; and ref.s.
    • (1991) Comprehensive Organic Synthesis , pp. 85-123
    • Ghosez, L.1    Marchand Brynaert, J.2
  • 10
    • 0003417469 scopus 로고    scopus 로고
    • 6.1
    • Several examples of related transformations are well represented in: Ghosez, L.; Marchand Brynaert, J. Comprehensive Organic Synthesis Trost, B. M.; Fleming, I.; Paquette, L. A. Eds., Pergamon Press, Oxford, 1991, 2.2, pp. 85-123; Durst, T.; Breau, T. ibid., 6.1, pp.675-694; Okamura, W. H.; De Lera, A. ibid., 6.2, pp. 699-745; and ref.s.
    • Comprehensive Organic Synthesis , pp. 675-694
    • Durst, T.1    Breau, T.I.2
  • 11
    • 0003417469 scopus 로고    scopus 로고
    • 6.2, and ref.s.
    • Several examples of related transformations are well represented in: Ghosez, L.; Marchand Brynaert, J. Comprehensive Organic Synthesis Trost, B. M.; Fleming, I.; Paquette, L. A. Eds., Pergamon Press, Oxford, 1991, 2.2, pp. 85-123; Durst, T.; Breau, T. ibid., 6.1, pp.675-694; Okamura, W. H.; De Lera, A. ibid., 6.2, pp. 699-745; and ref.s.
    • Comprehensive Organic Synthesis , pp. 699-745
    • Okamura, W.H.1    De Lera, A.I.2
  • 12
    • 0040975477 scopus 로고
    • Weissberger, A.; Taylor, E. C. Eds., John Wiley and Sons, Inc. New York, and ref.s.
    • Brown, D. J. The Chemistry of Heterocyclic Compounds, Weissberger, A.; Taylor, E. C. Eds., John Wiley and Sons, Inc. New York, 1985; 16, Suppl. II, pp.406-416 and ref.s.
    • (1985) The Chemistry of Heterocyclic Compounds , vol.16 , Issue.SUPPL. II , pp. 406-416
    • Brown, D.J.1
  • 13
    • 0003653439 scopus 로고
    • Oak Ridge National Laboratory, Tennessee, USA
    • Johnson, C.K. ORTEPII, Report ORNL-5138, 1976, Oak Ridge National Laboratory, Tennessee, USA.
    • (1976) ORTEPII, Report ORNL-5138
    • Johnson, C.K.1
  • 30
    • 0039196634 scopus 로고    scopus 로고
    • note
    • We also mention here that the thiadiazine ring of Ref. 18 carries a rather bulky ribofuranose moiety on the nitrogen in position 2 and yet the usual envelope conformation is adopted in this case also.
  • 36
    • 0010852875 scopus 로고
    • John Wiley and Sons, Inc. New York
    • Lindsay, R. O.; Allen, C. F. H. Organic Syntheses John Wiley and Sons, Inc. New York, 1955, Collective 3, p. 710.
    • (1955) Organic Syntheses , vol.COLLECTIVE 3 , pp. 710
    • Lindsay, R.O.1    Allen, C.F.H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.