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Volumn 5, Issue 4, 2003, Pages 399-402

Unusual, strained heterocycles: 3-Alkylidene-2-methyleneoxetanes from Morita-Baylis-Hillman-type adducts

Author keywords

[No Author keywords available]

Indexed keywords

ALLENE DERIVATIVE; DIMETHYLTITANOCENE; HETEROCYCLIC COMPOUND; LACTONE DERIVATIVE; OXETANE DERIVATIVE; TITANOCENE; UNCLASSIFIED DRUG;

EID: 0141518570     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol020202v     Document Type: Article
Times cited : (37)

References (41)
  • 10
    • 0011395825 scopus 로고
    • There are a number of reports in the literature of 3,4-dialkylideneoxetan-2-ones, which do contain a 2,3-dialkylideneoxetane substructure. However, these compounds will have a fundamentally different reactivity than the targeted dialkylideneoxetanes. For examples of the structurally related oxetanones, see: (a) Masters, A. P.; Sorensen, T. S. Tetrahedron Lett. 1989, 30, 5869-5872. (b) Zhidkova, T. A.; Vakulova, L. A.; Yanotovskii, M. T.; Svetlaeva, V. M.; Filippova, T. M. Pharm. Chem. J. (Engl. Transl.) 1983, 17, 344-346. (c) Baxter, G. J.; Brown, R. F. C.; Eastwood, F. W. ; Gatehouse, B. M.; Nesbit, M. C. Aust. J. Chem. 1978, 31, 1757-1767. (d) Payne, G. B. J. Org. Chem. 1966, 31, 718-721.
    • (1989) Tetrahedron Lett. , vol.30 , pp. 5869-5872
    • Masters, A.P.1    Sorensen, T.S.2
  • 11
    • 0020516295 scopus 로고
    • There are a number of reports in the literature of 3,4-dialkylideneoxetan-2-ones, which do contain a 2,3-dialkylideneoxetane substructure. However, these compounds will have a fundamentally different reactivity than the targeted dialkylideneoxetanes. For examples of the structurally related oxetanones, see: (a) Masters, A. P.; Sorensen, T. S. Tetrahedron Lett. 1989, 30, 5869-5872. (b) Zhidkova, T. A.; Vakulova, L. A.; Yanotovskii, M. T.; Svetlaeva, V. M.; Filippova, T. M. Pharm. Chem. J. (Engl. Transl.) 1983, 17, 344-346. (c) Baxter, G. J.; Brown, R. F. C.; Eastwood, F. W. ; Gatehouse, B. M.; Nesbit, M. C. Aust. J. Chem. 1978, 31, 1757-1767. (d) Payne, G. B. J. Org. Chem. 1966, 31, 718-721.
    • (1983) Pharm. Chem. J. (Engl. Transl.) , vol.17 , pp. 344-346
    • Zhidkova, T.A.1    Vakulova, L.A.2    Yanotovskii, M.T.3    Svetlaeva, V.M.4    Filippova, T.M.5
  • 12
    • 0141551130 scopus 로고
    • There are a number of reports in the literature of 3,4-dialkylideneoxetan-2-ones, which do contain a 2,3-dialkylideneoxetane substructure. However, these compounds will have a fundamentally different reactivity than the targeted dialkylideneoxetanes. For examples of the structurally related oxetanones, see: (a) Masters, A. P.; Sorensen, T. S. Tetrahedron Lett. 1989, 30, 5869-5872. (b) Zhidkova, T. A.; Vakulova, L. A.; Yanotovskii, M. T.; Svetlaeva, V. M.; Filippova, T. M. Pharm. Chem. J. (Engl. Transl.) 1983, 17, 344-346. (c) Baxter, G. J.; Brown, R. F. C.; Eastwood, F. W. ; Gatehouse, B. M.; Nesbit, M. C. Aust. J. Chem. 1978, 31, 1757-1767. (d) Payne, G. B. J. Org. Chem. 1966, 31, 718-721.
    • (1978) Aust. J. Chem. , vol.31 , pp. 1757-1767
    • Baxter, G.J.1    Brown, R.F.C.2    Eastwood, F.W.3    Gatehouse, B.M.4    Nesbit, M.C.5
  • 13
    • 0005065213 scopus 로고
    • There are a number of reports in the literature of 3,4-dialkylideneoxetan-2-ones, which do contain a 2,3-dialkylideneoxetane substructure. However, these compounds will have a fundamentally different reactivity than the targeted dialkylideneoxetanes. For examples of the structurally related oxetanones, see: (a) Masters, A. P.; Sorensen, T. S. Tetrahedron Lett. 1989, 30, 5869-5872. (b) Zhidkova, T. A.; Vakulova, L. A.; Yanotovskii, M. T.; Svetlaeva, V. M.; Filippova, T. M. Pharm. Chem. J. (Engl. Transl.) 1983, 17, 344-346. (c) Baxter, G. J.; Brown, R. F. C.; Eastwood, F. W. ; Gatehouse, B. M.; Nesbit, M. C. Aust. J. Chem. 1978, 31, 1757-1767. (d) Payne, G. B. J. Org. Chem. 1966, 31, 718-721.
    • (1966) J. Org. Chem. , vol.31 , pp. 718-721
    • Payne, G.B.1
  • 23
    • 0000892247 scopus 로고    scopus 로고
    • For reviews of the Baylis-Hillman reaction, see: (a) Ciganek, E. Org. React. 1997, 51, 201-350. (b) Basavaiah, D.; Rao, P. D.; Hyma, R. S. Tetrahedron 1996, 52, 8001-8062.
    • (1997) Org. React. , vol.51 , pp. 201-350
    • Ciganek, E.1
  • 24
    • 0342419508 scopus 로고    scopus 로고
    • For reviews of the Baylis-Hillman reaction, see: (a) Ciganek, E. Org. React. 1997, 51, 201-350. (b) Basavaiah, D.; Rao, P. D.; Hyma, R. S. Tetrahedron 1996, 52, 8001-8062.
    • (1996) Tetrahedron , vol.52 , pp. 8001-8062
    • Basavaiah, D.1    Rao, P.D.2    Hyma, R.S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.