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Volumn 61, Issue 19, 1996, Pages 6570-6574

1,3-dipolar activity in cycloadditions of an aliphatic sulfine

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EID: 0000118350     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo9607424     Document Type: Article
Times cited : (32)

References (36)
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    • For reviews, see: Block, E. Angew. Chem., Int. Ed. Engl. 1992, 31, 1135. Block, E. In Organic Sulfur Chemistry; Freidlina, R. Zh., Skorova, A. E., Eds.; Pergamon Press: Oxford, 1981; p 15.
    • (1992) Angew. Chem., Int. Ed. Engl. , vol.31 , pp. 1135
    • Block, E.1
  • 3
    • 0026756541 scopus 로고
    • Freidlina, R. Zh., Skorova, A. E., Eds.; Pergamon Press: Oxford
    • For reviews, see: Block, E. Angew. Chem., Int. Ed. Engl. 1992, 31, 1135. Block, E. In Organic Sulfur Chemistry; Freidlina, R. Zh., Skorova, A. E., Eds.; Pergamon Press: Oxford, 1981; p 15.
    • (1981) Organic Sulfur Chemistry , pp. 15
    • Block, E.1
  • 5
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    • For reviews, see: Zwanenburg, B.; Lenz, B. G. In Houben-Weyl, Methoden der Organischen Chemie; G. Thieme: Stuttgart, 1985; Vol. E 11, 911. Zwanenburg, B. Rec. Trav. Chim. Pays-Bas 1982, 101, 1.
    • (1982) Rec. Trav. Chim. Pays-Bas , vol.101 , pp. 1
    • Zwanenburg, B.1
  • 6
    • 0009385278 scopus 로고
    • S. Oae, Ed.; Plenum Press: New York
    • Bent, H. A. In Organic Chemistry of Sulfur; S. Oae, Ed.; Plenum Press: New York, 1977, p 1.
    • (1977) Organic Chemistry of Sulfur , pp. 1
    • Bent, H.A.1
  • 9
    • 0002481595 scopus 로고
    • Padwa, A., Ed.; Wiley: New York, (a) (b) p 139
    • For review, see: Huisgen R. In 1,3-Dipolar Cycloaddition Chemistry; Padwa, A., Ed.; Wiley: New York, 1984; Vol. 1, (a) p 2, (b) p 139.
    • (1984) 1,3-Dipolar Cycloaddition Chemistry , vol.1 , pp. 2
    • Huisgen, R.1
  • 11
    • 4243170543 scopus 로고    scopus 로고
    • We thank Prof. B. Zwanenburg, Nijmegen, for this private communication
    • We thank Prof. B. Zwanenburg, Nijmegen, for this private communication.
  • 12
    • 0001514996 scopus 로고
    • For reviews, see: (a) Kellogg, R. M. Tetrahedron 1976, 32, 2165. (b) Huisgen, R.; Fulka, C.; Kalwinsch, I.; Xi, L.; Mloston, G.; Moran, J. R.; Pröbstl, R. Bull. Soc. Chim. Belg. 1984, 93, 511.
    • (1976) Tetrahedron , vol.32 , pp. 2165
    • Kellogg, R.M.1
  • 24
    • 84943701775 scopus 로고
    • For reviews, see: (a) Sustmann, R. Pure Appl. Chem. 1974, 40, 569. (b) Houk, K. N. In Pericyclic Reactions; Marchand, A. P., Lehr, R. E., Eds.; Academic Press, Inc.: New York, 1977; Vol. 2, p 181. (c) Huisgen, R. J. Org. Chem. 1976, 41, 403.
    • (1974) Pure Appl. Chem. , vol.40 , pp. 569
    • Sustmann, R.1
  • 25
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    • Marchand, A. P., Lehr, R. E., Eds.; Academic Press, Inc.: New York
    • For reviews, see: (a) Sustmann, R. Pure Appl. Chem. 1974, 40, 569. (b) Houk, K. N. In Pericyclic Reactions; Marchand, A. P., Lehr, R. E., Eds.; Academic Press, Inc.: New York, 1977; Vol. 2, p 181. (c) Huisgen, R. J. Org. Chem. 1976, 41, 403.
    • (1977) Pericyclic Reactions , vol.2 , pp. 181
    • Houk, K.N.1
  • 26
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    • For reviews, see: (a) Sustmann, R. Pure Appl. Chem. 1974, 40, 569. (b) Houk, K. N. In Pericyclic Reactions; Marchand, A. P., Lehr, R. E., Eds.; Academic Press, Inc.: New York, 1977; Vol. 2, p 181. (c) Huisgen, R. J. Org. Chem. 1976, 41, 403.
    • (1976) J. Org. Chem. , vol.41 , pp. 403
    • Huisgen, R.1
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    • note
    • The authors have deposited the atomic coordinates for this structure with the Cambridge Crystallographic Data Centre. The coordinates can be obtained, on request, from the Director, Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 IEZ, U.K.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.