메뉴 건너뛰기




Volumn 69, Issue 18, 2004, Pages 5974-5985

Rearrangement of 4-(1-haloalkyl)- and 4-(2-haloalkyl)-2-azetidinones into methyl ω-alkylaminopentenoates via transient aziridines and azetidines

Author keywords

[No Author keywords available]

Indexed keywords

INTERMEDIATES; RING-OPENED PRODUCTS; STAUDINGER REACTION;

EID: 4344678639     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo040161b     Document Type: Article
Times cited : (37)

References (67)
  • 17
    • 4344575498 scopus 로고    scopus 로고
    • Japanese Kokai Tokkyo Koho JP 05 58,993 (Cl. C07D205/08), Mar 9, 1993, Appl. 91/246,759, Aug 30, 1991; Chem. Abstr. 1993, 119, 95311
    • (a) Kitatsume, T. Japanese Kokai Tokkyo Koho JP 05 58,993 (Cl. C07D205/08), Mar 9, 1993, Appl. 91/246,759, Aug 30, 1991; Chem. Abstr. 1993, 119, 95311.
    • Kitatsume, T.1
  • 20
    • 4344621168 scopus 로고    scopus 로고
    • PCT Int. Appl. WO 96 28, 421 (Cl. C07D205/08), Sep 19, 1996, JP Appl. 98/79,489, Mar 10, 1995
    • (d) Torii, S.; Tanaka, H.; Sasaoka, M.; Suzuki, D.; Kameyama, Y. PCT Int. Appl. WO 96 28, 421 (Cl. C07D205/08), Sep 19, 1996, JP Appl. 98/79,489, Mar 10, 1995; Chem. Abstr. 1996, 125, 328384.
    • (1996) Chem. Abstr. , vol.125 , pp. 328384
    • Torii, S.1    Tanaka, H.2    Sasaoka, M.3    Suzuki, D.4    Kameyama, Y.5
  • 21
    • 4344562515 scopus 로고
    • Canadian CA 1,128,530 (Cl. C07D205/08), Jul 27, 1982, U.S. Appl. 742,149, Nov 15, 1976
    • (e) Hall, R. F.; Huffman, W. F. Canadian CA 1,128,530 (Cl. C07D205/08), Jul 27, 1982, U.S. Appl. 742,149, Nov 15, 1976; Chem. Abstr. 1983, 98, 107066.
    • (1983) Chem. Abstr. , vol.98 , pp. 107066
    • Hall, R.F.1    Huffman, W.F.2
  • 22
    • 4344575206 scopus 로고
    • European Pat. Appl. EP 256,763 (Cl. C07D205/08), Feb 24, 1988, U.S. Appl. 893,748, Aug 6, 1986;
    • (f) Miller, M. J. European Pat. Appl. EP 256,763 (Cl. C07D205/08), Feb 24, 1988, U.S. Appl. 893,748, Aug 6, 1986;Chem. Abstr. 1988, 109, 6321.
    • (1988) Chem. Abstr. , vol.109 , pp. 6321
    • Miller, M.J.1
  • 24
    • 4344671440 scopus 로고
    • German Offen. 2,751,041 (Cl. C07D205/08), May 24, 1978, U.S. Appl. 742,149, Nov 15, 1976;
    • (h) Hall, R. F.; Huffman, W. F. German Offen. 2,751,041 (Cl. C07D205/08), May 24, 1978, U.S. Appl. 742,149, Nov 15, 1976; Chem. Abstr. 1979, 90, 103798.
    • (1979) Chem. Abstr. , vol.90 , pp. 103798
    • Hall, R.F.1    Huffman, W.F.2
  • 26
    • 4344676561 scopus 로고
    • (a) Fukumoto, K.; Ihara, M.; Takemura, M. Japanese Kokai Tokkyo Koho JP 04,266,869 (Cl. C07D205/08), Sep 22, 1992, Appl. 92/ 111,221, Feb 20, 1991; Chem. Abstr. 1993, 118, 101714.
    • (1993) Chem. Abstr. , vol.118 , pp. 101714
    • Fukumoto, K.1    Ihara, M.2    Takemura, M.3
  • 31
    • 4344709230 scopus 로고    scopus 로고
    • UK Patent Appl. GB 2,328,687 (Cl. C07D205/04), Mar 3, 1999, GB Appl. 1998/1,007, Jan 16, 1998
    • (f) Chung, J. Y. L.; Leazar, J. L.; Yasuda, N. UK Patent Appl. GB 2,328,687 (Cl. C07D205/04), Mar 3, 1999, GB Appl. 1998/1,007, Jan 16, 1998; Chem. Abstr. 1999,131, 5148.
    • (1999) Chem. Abstr. , vol.131 , pp. 5148
    • Chung, J.Y.L.1    Leazar, J.L.2    Yasuda, N.3
  • 32
    • 4344633982 scopus 로고    scopus 로고
    • PCT Int. Appl. WO 98 31,666 (Cl. C07D205/08), Jul, 1998, GB Appl. 97/5,855, Mar 21, 1997
    • (g) Yasuda, N.; Yang, C. PCT Int. Appl. WO 98 31,666 (Cl. C07D205/08), Jul, 1998, GB Appl. 97/5,855, Mar 21, 1997; Chem. Abstr. 1998, 129, 136022.
    • (1998) Chem. Abstr. , vol.129 , pp. 136022
    • Yasuda, N.1    Yang, C.2
  • 35
    • 4344666820 scopus 로고    scopus 로고
    • PCT Int. Appl. WO 96 28,453 (Cl. C07D513/04), Sep 19, 1996, JP Appl. 95/79,491, Mar 10, 1995
    • (j) Sasaoka, M.; Suzuki, D.; Suh, D.; Tokumaru, Y. PCT Int. Appl. WO 96 28,453 (Cl. C07D513/04), Sep 19, 1996, JP Appl. 95/79,491, Mar 10, 1995; Chem. Abstr. 1996, 125, 328385.
    • (1996) Chem. Abstr. , vol.125 , pp. 328385
    • Sasaoka, M.1    Suzuki, D.2    Suh, D.3    Tokumaru, Y.4
  • 49
    • 0013073080 scopus 로고    scopus 로고
    • Freeman, J. P., Ed.; John Wiley & Sons Inc.: New York
    • Hubschwerlen, C.; Specklin, J.-L. In Organic Synthesis; Freeman, J. P., Ed.; John Wiley & Sons Inc.: New York, 1998; Collect. Vol. IX, p 13.
    • (1998) Organic Synthesis , vol.9 , pp. 13
    • Hubschwerlen, C.1    Specklin, J.-L.2
  • 62
    • 0002102562 scopus 로고
    • β-lactam synthon method: Enantiomerically pure β-lactams as synthetic intermediates
    • Georg, G. I., Ed.; VCH: New York; Chapter 4, and references cited therein
    • Ojima, I. β-Lactam Synthon Method: Enantiomerically Pure β-Lactams as Synthetic Intermediates. In The Organic Chemistry of β-Lactams; Georg, G. I., Ed.; VCH: New York, 1993; Chapter 4, pp 197-255 and references cited therein.
    • (1993) The Organic Chemistry of β-Lactams , pp. 197-255
    • Ojima, I.1
  • 66
    • 4344621169 scopus 로고    scopus 로고
    • (b) http://www.spectroscopynow.com/Spy/tools/proton-proton.html.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.